Version: 3.17

Nirvana JSON File Format

Overview

Conventions

In the Nirvana JSON representation, we try to maximize the amount of useful information that is relayed in the output file. As such, we have several conventions that are useful to know about:

With boolean key/value pairs, we only output the keys that have a true value. I.e. there's no reason to display "isStructuralVariant":false a few million times when annotating a small variant VCF.
When transferring data from the VCF file to the JSON (e.g. for allele depths (AD)), it is common to use a period (.) as a placeholder for missing data in the VCF file. Nirvana treats periods like empty or null strings and therefore will not output those entries.

JSON Layout

info

In general, each position corresponds to a row in the original VCF file.

For each gene that was referenced in the transcripts found in the positions section, there will be additional gene-level annotation in the gene section.

Parsing

info

We've put together a new section that discusses how to parse our JSON files easily using examples in a Python Jupyter notebook and a R version as well. In addition, we have information about how to quickly dump content from our JSON file using a tabix-like utility called JASIX.

{
   "header":{
      "annotator":"Nirvana 3.0.0-alpha.5+g6c52e247",
      "creationTime":"2017-06-14 15:53:13",
      "genomeAssembly":"GRCh37",
      "dataSources":[
         {
            "name":"OMIM",
            "version":"unknown",
            "description":"An Online Catalog of Human Genes and Genetic Disorders",
            "releaseDate":"2017-05-03"
         },
         {
            "name":"VEP",
            "version":"84",
            "description":"BothRefSeqAndEnsembl",
            "releaseDate":"2017-01-16"
         },
         {
            "name":"ClinVar",
            "version":"20170503",
            "description":"A freely accessible, public archive of reports of the relationships among human variations and phenotypes, with supporting evidence",
            "releaseDate":"2017-05-03"
         },
         {
            "name":"phyloP",
            "version":"hg19",
            "description":"46 way conservation score between humans and 45 other vertebrates",
            "releaseDate":"2009-11-10"
         }
      ],
      "samples":[
         "NA12878",
         "NA12891",
         "NA12892"
      ]
   },

Field	Type	Notes
annotator	string	the name of the annotator and the current version
creationTime	string	yyyy-MM-dd hh:mm:ss
genomeAssembly	string	see possible values below
schemaVersion	integer	incremented whenever the core structure of the JSON file introduces breaking changes
dataVersion	string
dataSources	object array	see Data Source entry below
samples	string array	the order of these sample names will be used throughout the JSON file when enumerating samples

Data Source

Field	Type	Notes
name	string
version	string
description	string	optional description of the data source
releaseDate	string	yyyy-MM-dd

Genome Assemblies

GRCh37
GRCh38
hg19
SARSCoV2

Positions

"positions":[
   {
      "chromosome":"chr2",
      "position":48010488,
      "repeatUnit":"GGCCCC",
      "refRepeatCount":3,
      "svEnd":48020488,
      "refAllele":"G",
      "altAlleles":[
         "A",
         "GT"
      ],
      "quality":461,
      "filters":[
         "PASS"
      ],
      "ciPos":[
         -170,
         170
      ],
      "ciEnd":[
         -175,
         175
      ],
      "svLength":1000,
      "strandBias":1.23,
      "jointSomaticNormalQuality":29,
      "cytogeneticBand":"2p16.3",

Field	Type	Variant Type	Notes
chromosome	string	all	exactly as displayed in the vcf
position	integer	all	exactly as displayed in the vcf (1-based notation). Range: 1 - 250 million
repeatUnit	string	STR	provided by ExpansionHunter
refRepeatCount	integer	STR	provided by ExpansionHunter
svEnd	integer	SV
refAllele	string	all	exactly as displayed in the vcf
altAllele	string array	all	exactly as displayed in the vcf
quality	float	all	exactly as displayed in the vcf (Normally an integer, but some variant callers using floating point. Has been observed as high as 500k)
filters	string array	all	exactly as displayed in the vcf
ciPos	integer array	SV
ciEnd	integer array	SV
svLength	integer	SV
strandBias	float	small variant	provided by GATK (from SB)
jointSomaticNormalQuality	integer	SV	provided by the Manta variant caller (SOMATICSCORE)
cytogeneticBand	string	all	e.g. 17p13.1

ClinGen

"clingen":[
   {
      "chromosome":"17",
      "begin":525,
      "end":14667519,
      "variantType":"copy_number_gain",
      "id":"nsv996083",
      "clinicalInterpretation":"pathogenic",
      "observedGains":1,
      "validated":true,
      "phenotypes":[
         "Intrauterine growth retardation"
      ],
      "phenotypeIds":[
         "HP:0001511",
         "MedGen:C1853481"
      ],
      "reciprocalOverlap":0.00131
   },
   {
      "chromosome":"17",
      "begin":45835,
      "end":7600330,
      "variantType":"copy_number_loss",
      "id":"nsv869419",
      "clinicalInterpretation":"pathogenic",
      "observedLosses":1,
      "validated":true,
      "phenotypes":[
         "Developmental delay AND/OR other significant developmental or morphological phenotypes"
      ],
      "reciprocalOverlap":0.00254
   }
]

Field	Type	Notes
clingen	object array
chromosome	string	Ensembl-style chromosome names
begin	integer	1-based position
end	integer	1-based position
variantType	string	Any of the sequence alterations defined here.
id	string	Identifier from the data source. Alternatively a VID
clinicalInterpretation	string	see possible values below
observedGains	integer	Range: 0 - (2³¹ - 1). Only used if copy_number_variation, copy_number_loss, or copy_number_gain.
observedLosses	integer	Range: 0 - (2³¹ - 1). Only used if copy_number_variation, copy_number_loss, or copy_number_gain.
validated	boolean
phenotypes	string array	Description of the phenotype.
phenotypeIds	string array	Description of the phenotype IDs.
reciprocalOverlap	floating point	Range: 0 - 1. E.g. 0.57 would indicate a 57% reciprocal overlap. Specified up to 5 decimal places (Not reported for Insertions).

clinicalInterpretation

benign
curated benign
curated pathogenic
likely benign
likely pathogenic
path gain
path loss
pathogenic
uncertain

"clingenDosageSensitivityMap": [{
    "chromosome": "15",
    "begin": 30900686,
    "end": 32153204,
    "haploinsufficiency": "sufficient evidence suggesting dosage sensitivity is associated with clinical phenotype",
    "triplosensitivity": "little evidence suggesting dosage sensitivity is associated with clinical phenotype",
    "reciprocalOverlap": 0.00147,
    "annotationOverlap": 0.33994
},
{
    "chromosome": "15",
    "begin": 31727418,
    "end": 32153204,
    "haploinsufficiency": "sufficient evidence suggesting dosage sensitivity is associated with clinical phenotype",
    "triplosensitivity": "dosage sensitivity unlikely",
    "reciprocalOverlap": 0.00147,
    "annotationOverlap": 1
}]

Field	Type	Notes
clingenDosageSensitivityMap	object array
chromosome	string	Ensembl-style chromosome names
begin	integer	1-based position
end	integer	1-based position
haploinsufficiency	string	see possible values below
triplosensitivity	string	(same as haploinsufficiency)
reciprocalOverlap	floating point	Range: 0 - 1. E.g. 0.57 would indicate a 57% reciprocal overlap. Specified up to 5 decimal places (Not reported for Insertions).
annotationOverlap	floating point	Range: 0 - 1. E.g. 0.57 would indicate a 57% reciprocal overlap. Specified up to 5 decimal places (Not reported for Insertions).

haploinsufficiency and triplosensitivity

no evidence to suggest that dosage sensitivity is associated with clinical phenotype
little evidence suggesting dosage sensitivity is associated with clinical phenotype
emerging evidence suggesting dosage sensitivity is associated with clinical phenotype
sufficient evidence suggesting dosage sensitivity is associated with clinical phenotype
gene associated with autosomal recessive phenotype
dosage sensitivity unlikely

1000 Genomes (SV)

"oneKg":[
   {
      "chromosome":"1",
      "begin":1595369,
      "end":1612441,
      "variantType": "copy_number_variation",
      "id": "esv3635753;esv3635754;esv3635755;esv3635756;esv3635757",
      "allAn": 5008,
      "allAc": 2702,
      "allAf": 0.539537,
      "afrAf": 0.6052,
      "amrAf": 0.3675,
      "eurAf": 0.5357,
      "easAf": 0.5368,
      "sasAf": 0.5797,
      "reciprocalOverlap": 0.07555
   }
],

Field	Type	Notes
chromosome	string
begin	integer
end	integer
variantType	string
id	string
allAn	floating point	allele number for all populations. Non-zero integer.
allAc	floating point	allele count for all populations. Integer.
allAf	floating point	allele frequency for all populations. Range: 0 - 1.0
afrAf	floating point	allele frequency for the African super population. Range: 0 - 1.0
amrAf	floating point	allele frequency for the Ad Mixed American super population. Range: 0 - 1.0
eurAf	floating point	allele frequency for the European super population. Range: 0 - 1.0
easAf	integer	allele frequency for the East Asian super population. Range: 0 - 1.0
sasAf	integer	allele frequency for the South Asian super population. Range: 0 - 1.0
reciprocalOverlap	floating point	range: 0 - 1.

MITOMAP (SV)

"mitomap":[ 
   { 
      "chromosome":"MT",
      "begin":3166,
      "end":14152,
      "variantType":"deletion",
      "reciprocalOverlap":0.18068,
      "annotationOverlap":0.42405
   }
]

Field	Type	Notes
chromosome	string
begin	integer
end	integer
variantType	string array
reciprocalOverlap	float	Range: 0 - 1. Specified up to 5 decimal places
annotationOverlap	float	Range: 0 - 1. Specified up to 5 decimal places

Samples

"samples":[
   {
      "genotype":"0/1",
      "variantFrequencies":[
         0.333,
         0.5
      ],
      "totalDepth":57,
      "genotypeQuality":12,
      "copyNumber":3,
      "repeatUnitCounts":[
         10,
         20
      ],
      "alleleDepths":[
         10,
         20,
         30
      ],
      "failedFilter":true,
      "splitReadCounts":[
         10,
         20
      ],
      "pairedEndReadCounts":[
         10,
         20
      ],
      "isDeNovo":true,
      "diseaseAffectedStatuses":[
         "-"
      ],
      "artifactAdjustedQualityScore":89.3,
      "likelihoodRatioQualityScore":78.2,
      "heteroplasmyPercentile":[
         23.13,
         12.65
      ]
   }
]

Field	Type	VCF	Notes
genotype	string	GT
variantFrequencies	float array	VF, AD	range: 0 - 1.0. One value per alternate allele
totalDepth	integer	DP	non-negative integer values
genotypeQuality	integer	GQ	non-negative integer values. Typically maxes out at 99
copyNumber	integer	CN	non-negative integer values
minorHaplotypeCopyNumber	integer	MCN	non-negative integer values
repeatUnitCounts	integer array	REPCN	ExpansionHunter-specific
alleleDepths	integer array	AD	non-negative integer values
failedFilter	bool	FT
splitReadCounts	integer array	SR	Manta-specific
pairedEndReadCounts	integer array	PR	Manta-specific
isDeNovo	bool	DN
deNovoQuality	float	DQ
diseaseAffectedStatuses	string array	DST	ExpansionHunter-specific
artifactAdjustedQualityScore	float	AQ	PEPE-specific. Range: 0 - 100.0
likelihoodRatioQualityScore	float	LQ	PEPE-specific. Range: 0 - 100.0
lossOfHeterozygosity	bool	CN, MCN
somaticQuality	float	SQ
heteroplasmyPercentile	float	VF	range: 0 - 100. 2 decimal places. One value per alternate allele
binCount	integer	BC	non-negative integer values

Empty Samples

If a sample does not contain any entries, we will create a sample object that contains the isEmpty key. This ensures that sample ordering is preserved while indicating that a sample is intentionally empty.

"samples":[
   {
      "isEmpty":true
   }
],

Variants

"variants":[
   {
      "vid":"2:48010488:A",
      "chromosome":"chr2",
      "begin":48010488,
      "end":48010488,
      "isReferenceMinorAllele":true,
      "isStructuralVariant":true,
      "refAllele":"G",
      "altAllele":"A",
      "variantType":"SNV",
      "isDecomposedVariant":true,
      "isRecomposedVariant":true,
      "linkedVids":["2:48010488:GTA:ATC"],
      "hgvsg":"NC_000002.11:g.48010488G>A",
      "phylopScore":0.459

Field	Type	Notes
vid	string	see Variant Identifiers
chromosome	string
begin	int	1-based non-negative integer values. Range: 1 - 250 million
end	int	1-based non-negative integer values. Range: 1 - 250 million
isReferenceMinorAllele	bool	true when this is a reference minor allele
isStructuralVariant	bool	true when the variant is a structural variant
inLowComplexityRegion	bool	true when the variant lies in a low complexity region (gnomAD low complexity regions)
refAllele	string	parsimonious representation of the reference allele
altAllele	string	parsimonious representation of the alternate allele.
variantType	string	uses Sequence Ontology sequence alterations
isDecomposedVariant	bool	true when the decomposed variant has been used to create another recomposed variant
isRecomposedVariant	bool	true when the variant is recomposed from two or more decomposed variants
linkedVids	string array	list of VIDs for variants connecting decomposed and recomposed variants
hgvsg	string	HGVS g. notation
phylopScore	float	phyloP conservation score. Range: -14.08 to 6.424

Reference Minor Alleles

Nirvana supports annotating reference minor alleles. In such a case, refAllele will be replaced by the global major allele and altAllele will be replaced with the original reference allele.

Flagging Decomposed & Recomposed Variants

When two or more decomposed variants are recomposed into an MNV, the decomposed variants will be marked with "isDecomposedVariant":true.

Similarly, the recomposed variant will be shown as a new VCF position. This recomposed variant will be flagged with "isRecomposedVariant":true.

Transcripts

"transcripts":[
   {
      "transcript":"ENST00000445503.1",
      "source":"Ensembl",
      "bioType":"nonsense_mediated_decay",
      "codons":"gGg/gAg",
      "aminoAcids":"G/E",
      "cdnaPos":"268",
      "cdsPos":"116",
      "exons":"1/9",
      "introns":"1/8",
      "proteinPos":"39",
      "geneId":"ENSG00000116062",
      "hgnc":"MSH6",
      "consequence":[
         "missense_variant",
         "NMD_transcript_variant"
      ],
      "hgvsc":"ENST00000445503.1:c.116G>A",
      "hgvsp":"ENSP00000405294.1:p.(Gly39Glu)",
      "geneFusion":{
         "exon":6,
         "intron":5,
         "fusions":[
            {
               "hgvsc":"ETV6{ENST00000396373.4}:c.1_1009+3402_RUNX1{ENST00000437180.1}:c.58+568_1443",
               "exon":3,
               "intron":2
            },
            {
               "hgvsc":"ETV6{ENST00000396373.4}:c.1_1009+3402_RUNX1{ENST00000300305.3}:c.58+568_1443",
               "exon":2,
               "intron":1
            }
         ]
      },
      "isCanonical":true,
      "polyPhenScore":0.95,
      "polyPhenPrediction":"probably damaging",
      "proteinId":"ENSP00000405294.1",
      "siftScore":0.61,
      "siftPrediction":"tolerated",
      "completeOverlap":true
   }
]

Field	Type	Notes
transcript	string	transcript ID. e.g. ENST00000445503.1
source	string	RefSeq / Ensembl
bioType	string	descriptions of the biotypes from Ensembl
codons	string
aminoAcids	string
cdnaPos	string
cdsPos	string
exons	string	exons affected by the variant
introns	string	introns affected by the variant
proteinPos	string
geneId	string	gene ID. e.g. ENSG00000116062
hgnc	string	gene symbol. e.g. MSH6
consequence	string array	Sequence Ontology Consequences
hgvsc	string	HGVS coding nomenclature
hgvsp	string	HGVS protein nomenclature
geneFusion	object	see Gene Fusions entry below
isCanonical	bool	true when this is a canonical transcript
polyPhenScore	float	range: 0 - 1.0
polyPhenPrediction	string	see possible values below
proteinId	string	protein ID. E.g. ENSP00000405294.1
siftScore	float	range: 0 - 1.0
siftPrediction	string	see possible values below
completeOverlap	bool	true when this transcript is completely overlapped by the variant

PolyPhen

probably damaging
possibly damaging
benign
unknown

SIFT

tolerated
deleterious
tolerated - low confidence
deleterious - low confidence

Amino Acid Conservation

"aminoAcidConservation": {
    "scores": [0.34]
}

Field	Type	Notes
aminoAcidConservation	object
scores	object array of doubles	percent conserved with respect to human amino acid residue. Range: 0.01 - 1.00

Gene Fusions

Field	Type	Notes
exon	int	actual exon where the breakpoint was located
intron	int	actual intron where the breakpoint was located
fusions	object array	see Fusion entry below

Fusion

Field	Type	Notes
exon	int	actual exon where the other breakpoint was located
intron	int	actual intron where the other breakpoint was located
hgvsc	string	HGVS coding nomenclature describing the two genes and the transcripts that are fused along with

Regulatory Regions

"regulatoryRegions":[
   {
      "id":"ENSR00001542175",
      "type":"promoter",
      "consequence":[
         "regulatory_region_variant"
      ]
   }
]

Field	Type	Notes
id	string
type	string	see possible values below
consequence	string array	see possible values below

Regulatory Types

CTCF_binding_site
enhancer
open_chromatin_region
promoter
promoter_flanking_region
TF_binding_site

Regulatory Consequences

regulatory_region_variant
regulatory_region_ablation
regulatory_region_amplification
regulatory_region_truncation

ClinVar

"clinvar":[
   {
      "id":"VCV000036581.3",
      "reviewStatus":"reviewed by expert panel",
      "significance":[
         "benign"
      ],
      "refAllele":"G",
      "altAllele":"A",
      "lastUpdatedDate":"2020-03-01",
      "isAlleleSpecific":true
   },
   {
      "id":"RCV000030258.4",
      "variationId":"VCV000036581.3",
      "reviewStatus":"reviewed by expert panel",
      "alleleOrigins":[
         "germline"
      ],
      "refAllele":"G",
      "altAllele":"A",
      "phenotypes":[
         "Lynch syndrome"
      ],
      "medGenIds":[
         "C1333990"
      ],
      "omimIds":[
         "120435"
      ],
      "significance":[
         "benign"
      ],
      "lastUpdatedDate":"2017-05-01",
      "isAlleleSpecific":true
   }
]

Field	Type	Notes
id	string	ClinVar ID
variationId	string	ClinVar VCV ID
reviewStatus	string	see possible values below
alleleOrigins	string array	see possible values below
refAllele	string
altAllele	string
phenotypes	string array
medGenIds	string array	MedGen IDs
omimIds	string array	OMIM IDs
orphanetIds	string array	Orphanet IDs
significance	string array	see possible values below
lastUpdatedDate	string	yyyy-MM-dd
pubMedIds	string array	PubMed IDs
isAlleleSpecific	bool	true when the current variant alternate allele matches the ClinVar alternate allele

reviewStatus:

no assertion provided
no assertion criteria provided
criteria provided, single submitter
practice guideline
classified by multiple submitters
criteria provided, conflicting interpretations
criteria provided, multiple submitters, no conflicts
no interpretation for the single variant

alleleOrigins:

unknown
other
germline
somatic
inherited
paternal
maternal
de-novo
biparental
uniparental
not-tested
tested-inconclusive

significance:

uncertain significance
not provided
benign
likely benign
likely pathogenic
pathogenic
drug response
histocompatibility
association
risk factor
protective
affects
conflicting data from submitters
other
no interpretation for the single variant
conflicting interpretations of pathogenicity

1000 Genomes

"oneKg":{
   "allAf":0.200879,
   "afrAf":0.210287,
   "amrAf":0.139769,
   "easAf":0.275794,
   "eurAf":0.181909,
   "sasAf":0.173824,
   "allAn":5008,
   "afrAn":1322,
   "amrAn":694,
   "easAn":1008,
   "eurAn":1006,
   "sasAn":978,
   "allAc":1006,
   "afrAc":278,
   "amrAc":97,
   "easAc":278,
   "eurAc":183,
   "sasAc":170
}

Field	Type	Notes
allAf	float	allele frequency for all populations. Range: 0 - 1.0
allAc	int	allele count for all populations. Integer.
allAn	int	allele number for all populations. Non-zero integer.
afrAf	float	allele frequency for the African super population. Range: 0 - 1.0
afrAc	int	allele count for the African super population. Integer.
afrAn	int	allele number for the African super population. Non-zero integer.
amrAf	float	allele frequency for the Ad Mixed American super population. Range: 0 - 1.0
amrAc	int	allele count for the Ad Mixed American super population. Integer.
amrAn	int	allele number for the Ad Mixed American super population. Non-zero integer.
easAf	float	allele frequency for the East Asian super population. Range: 0 - 1.0
easAc	int	allele count for the East Asian super population. Integer.
easAn	int	allele number for the East Asian super population. Non-zero integer.
eurAf	float	allele frequency for the European super population. Range: 0 - 1.0
eurAc	int	allele count for the European super population. Integer.
eurAn	int	allele number for the European super population. Non-zero integer.
sasAf	float	allele frequency for the South Asian super population. Range: 0 - 1.0
sasAc	int	allele count for the South Asian super population. Integer.
sasAn	int	allele number for the South Asian super population. Non-zero integer.

gnomAD

"gnomad":{ 
   "coverage":20,
   "allAf":0.190317,
   "maleAf":0.193,
   "femaleAf": 0.1935,
   "afrAf":0.222876,
   "amrAf":0.121394,
   "easAf":0.239802,
   "finAf":0.136833,
   "nfeAf":0.181282,
   "asjAf":0.258278,
   "othAf":0.186094,
   "allAn":30796,
   "maleAn":15096,
   "femaleAn":15700
   "afrAn":8664,
   "amrAn":832,
   "easAn":1618,
   "finAn":3486,
   "nfeAn":14916,
   "asjAn":302,
   "othAn":978,
   "allAc":5861,
   "maleAc":2930,
   "femaleAc": 2931,
   "afrAc":1931,
   "amrAc":101,
   "easAc":388,
   "finAc":477,
   "nfeAc":2704,
   "asjAc":78,
   "othAc":182,
   "allHc":561,
   "afrHc":208,
   "amrHc":6,
   "easHc":42,
   "finHc":31,
   "nfeHc":242,
   "asjHc":13,
   "othHc":19,
   "maleHc":280,
   "femaleHc":281,
   "controlsAllAf":0.190317,
   "controlsAllAn":30796,
   "controlsAllAc":5861,
   "lowComplexityRegion":true,
   "failedFilter":true
}

Field	Type	Notes
coverage	int	average coverage (non-negative integer values)
allAf	float	allele frequency for all populations. Range: 0 - 1.0
maleAf	float	allele frequency for male population. Range: 0 - 1.0
femaleAf	float	allele frequency for female population. Range: 0 - 1.0
controlsAllAf	float	allele frequency for the controls subset. Range: 0 - 1.0
allAc	int	allele count for all populations. Integer.
maleAc	int	allele count for male population. Integer.
femaleAc	int	allele count for female population. Integer.
controlsAllAc	int	allele count for the controls subset. Integer.
allAn	int	allele number for all populations. Non-zero integer.
maleAn	int	allele number for male population. Non-zero integer.
femaleAn	int	allele number for female population. Non-zero integer.
controlsAllAn	int	allele number for the controls subset. Non-zero integer.
allHc	int	count of homozygous individuals for all populations. Non-negative integer.
maleHc	int	count of homozygous individuals for male population. Non-negative integer.
femaleHc	int	count of homozygous individuals for female population. Non-negative integer.
afrAf	float	allele frequency for the African / African American population. Range: 0 - 1.0
afrAc	int	allele count for the African / African American population. Integer.
afrAn	int	allele number for the African / African American population. Non-zero integer.
afrHc	int	count of homozygous individuals for African / African American population. Non-negative integer.
amrAf	float	allele frequency for the Latino population. Range: 0 - 1.0
amrAc	int	allele count for the Latino population. Integer.
amrAn	int	allele number for the Latino population. Non-zero integer.
amrHc	int	count of homozygous individuals for Latino population. Non-negative integer.
easAf	float	allele frequency for the East Asian population. Range: 0 - 1.0
easAc	int	allele count for the East Asian population. Integer.
easAn	int	allele number for the East Asian population. Non-zero integer.
easHc	int	count of homozygous individuals for East Asian population. Non-negative integer.
finAf	float	allele frequency for the Finnish population. Range: 0 - 1.0
finAc	int	allele count for the Finnish population. Integer.
finAn	int	allele number for the Finnish population. Non-zero integer.
finHc	int	count of homozygous individuals for Finnish population. Non-negative integer
nfeAf	float	allele frequency for the Non-Finnish European population. Range: 0 - 1.0
nfeAc	int	allele count for the Non-Finnish European population. Integer.
nfeAn	int	allele number for the Non-Finnish European population. Non-zero integer.
nfeHc	int	count of homozygous individuals for Non-Finnish European population. Non-negative integer
othAf	float	allele frequency for the Other population. Range: 0 - 1.0
othAc	int	allele count for the Other population. Integer.
othAn	int	allele number for the Other population. Non-zero integer.
othHc	int	count of homozygous individuals for Other population. Non-negative integer
asjAf	float	allele frequency for the Ashkenazi Jewish population. Range: 0 - 1.0
asjAc	int	allele count for the Ashkenazi Jewish population Integer.
asjAn	int	allele number for the Ashkenazi Jewish population. Non-zero integer.
asjHc	int	count of homozygous individuals for the Ashkenazi Jewish population. Non-negative integer
sasAf	float	allele frequency for the South Asian population. Range: 0 - 1.0
sasAc	int	allele count for the South Asian population Integer.
sasAn	int	allele number for the South Asian population. Non-zero integer.
sasHc	int	count of homozygous individuals for the South Asian population. Non-negative integer.
failedFilter	bool	True if this variant failed any filters (Note: we do not list the failed filters)
lowComplexityRegion	bool	True if this variant is located in a low complexity region.

dbSNP

"dbsnp":[
   "rs1042821"
]

Field	Type	Notes
dbsnp	string array	dbSNP rsIDs

MITOMAP

"mitomap":[ 
   { 
      "refAllele":"G",
      "altAllele":"A",
      "diseases":[ 
         "Bipolar disorder",
         "Melanoma"
      ],
      "hasHomoplasmy":false,
      "hasHeteroplasmy":true,
      "status":"Reported",
      "clinicalSignificance":"confirmed pathogenic",
      "scorePercentile":83.30,
      "numGenBankFullLengthSeqs":2,
      "pubMedIds":["2316527","6299878","6301949"],
      "isAlleleSpecific":true
   }
]

Field	Type	Notes
refAllele	string
altAllele	string
diseases	string array	associated diseases
hasHomoplasmy	boolean
hasHeteroplasmy	boolean
status	string	record status
clinicalSignificance	string	predicted pathogenicity
scorePercentile	float	MitoTIP score
numGenBankFullLengthSeqs	integer	# of GenBank full-length sequences
pubMedIds	string array
isAlleleSpecific	boolean	true when the current variant alternate allele matches the MITOMAP alternate allele

Primate AI

"primateAI":[
   {
      "hgnc":"TP53",
      "scorePercentile":0.3,
   }
]

Field	Type	Notes
hgnc	string
scorePercentile	float	range: 0 - 1.0

REVEL

"revel":{ 
   "score":0.027
}

Field	Type	Notes
score	float	Range: 0 - 1.0

Splice AI

"spliceAI":[ 
   {
      "hgnc":"BLCAP",
      "acceptorGainDistance":-3,
      "acceptorGainScore":0.3,
      "donorLossDistance":7,
      "donorLossScore":0.9
   },
   { 
      "hgnc":"NNAT",
      "acceptorGainDistance":-1,
      "acceptorGainScore":0.2,
      "donorGainDistance":-2,
      "donorGainScore":0.3
   }
]

Field	Type	Notes
hgnc	string	HGNC gene symbol
acceptorGainDistance	int	± bp from current position
acceptorGainScore	float	range: 0 - 1.0. 1 decimal place
acceptorLossDistance	int	± bp from current position
acceptorLossScore	float	range: 0 - 1.0. 1 decimal place
donorGainDistance	int	± bp from current position
donorGainScore	float	range: 0 - 1.0. 1 decimal place
donorLossDistance	int	± bp from current position
donorLossScore	float	range: 0 - 1.0. 1 decimal place

TOPMed

"topmed":{ 
   "allAc":20,
   "allAn":125568,
   "allAf":0.000159,
   "allHc":0,
   "failedFilter":true
}

Field	Type	Notes
allAc	int	TOPMed allele count
allAn	int	TOPMed allele number. Non-zero integer.
allAf	float	TOPMed allele frequency (computed by Nirvana)
allHc	int	TOPMed homozygous count
failedFilter	bool	True if this variant failed any filters

Genes

"genes":[
   {
      "name":"MSH6",
      "hgncId":7329,
      "summary":"This gene encodes a member of the DNA mismatch repair MutS family. In E. coli, the MutS protein helps in the recognition of mismatched nucleotides prior to their repair. A highly conserved region of approximately 150 aa, called the Walker-A adenine nucleotide binding motif, exists in MutS homologs. The encoded protein heterodimerizes with MSH2 to form a mismatch recognition complex that functions as a bidirectional molecular switch that exchanges ADP and ATP as DNA mismatches are bound and dissociated. Mutations in this gene may be associated with hereditary nonpolyposis colon cancer, colorectal cancer, and endometrial cancer. Transcripts variants encoding different isoforms have been described. [provided by RefSeq, Jul 2013]",
      /* this is where gene-level data sources can be found e.g. OMIM */
   }
]

Field	Type	Notes
name	string	HGNC gene symbol
hgncId	int	HGNC ID
summary	string	short description of the gene from OMIM

OMIM

"omim":[ 
   { 
      "mimNumber":600678,
      "geneName":"MutS, E. coli, homolog of, 6",
      "description":"The transcription factor p53 responds to diverse cellular stresses to regulate target genes that induce cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. In addition, p53 appears to induce apoptosis through nontranscriptional cytoplasmic processes. In unstressed cells, p53 is kept inactive essentially through the actions of the ubiquitin ligase MDM2, which inhibits p53 transcriptional activity and ubiquitinates p53 to promote its degradation. Numerous posttranslational modifications modulate p53 activity, most notably phosphorylation and acetylation. Several less abundant p53 isoforms also modulate p53 activity. Activity of p53 is ubiquitously lost in human cancer either by mutation of the p53 gene itself or by loss of cell signaling upstream or downstream of p53 (Toledo and Wahl, 2006; Bourdon, 2007; Vousden and Lane, 2007)",
      "phenotypes":[ 
         { 
            "mimNumber":614350,
            "phenotype":"Colorectal cancer, hereditary nonpolyposis, type 5",
            "description":"Hereditary nonpolyposis colorectal cancer type 5 is a cancer predisposition syndrome ...",
            "mapping":"molecular basis of the disorder is known",
            "inheritances":[ 
               "Autosomal dominant"
            ]
         },
         { 
            "mimNumber":608089,
            "phenotype":"Endometrial cancer, familial",
            "mapping":"molecular basis of the disorder is known"
         },
         { 
            "mimNumber":276300,
            "phenotype":"Mismatch repair cancer syndrome",
            "description":"Constitutional mismatch repair deficiency is a rare childhood cancer predisposition syndrome ...",
            "mapping":"molecular basis of the disorder is known",
            "inheritances":[ 
               "Autosomal recessive"
            ],
            "comments"     : [
                "contribute to susceptibility to multifactorial disorders or to susceptibility to infection",
                "unconfirmed or possibly spurious mapping"
            ]
         }
      ]
   }
]

Field	Type	Notes
mimNumber	int	OMIM ID for gene
geneName	string	gene name
description	string
phenotypes	object array	see Phenotype entry below

Phenotype

Field	Type	Notes
mimNumber	int
phenotype	string
description	string
mapping	string	see possible values below
inheritance	string array	see possible values below
comments	string array	see possible values below

Mapping

disorder was positioned by mapping of the wild type gene
disease phenotype itself was mapped
molecular basis of the disorder is known
disorder is a chromosome deletion or duplication syndrome

Inheritance

autosomal recessive
autosomal dominant

Comments

contributes to the susceptibility to multifactorial disorders
variations that lead to apparently abnormal laboratory test values
unconfirmed mapping

gnomAD LoF Gene Metrics

"gnomAD":{ 
   "pLi":1.00e0,
   "pNull":8.94e-40,
   "pRec":1.84e-16,
   "synZ":-8.44e-2,
   "misZ":5.96e-1,
   "loeuf":1.13e0
}

Field	Type	Notes
pLi	float	probability of being intolerant of a single loss-of-function variant (like haploinsufficient genes, observed ~ 0.1*expected)
pNull	float	probability of being completely tolerant of loss of function variation (observed = expected)
pRec	float	probability of being intolerant of two loss of function variants (like recessive genes, observed ~ 0.5*expected)
synZ	float	corrected synonymous Z score
misZ	float	corrected missense Z score
loeuf	float	loss of function observed/expected upper bound fraction (LOEUF)

ClinGen Disease Validity

"clingenGeneValidity":[
   {
      "diseaseId":"MONDO_0007893",
      "disease":"Noonan syndrome with multiple lentigines",
      "classification":"no reported evidence",
      "classificationDate":"2018-06-07"
   },
   {
      "diseaseId":"MONDO_0015280",
      "disease":"cardiofaciocutaneous syndrome",
      "classification":"no reported evidence",
      "classificationDate":"2018-06-07"
   }
]

Field	Type	Notes
clingenGeneValidity	object
diseaseId	string	Monarch Disease Ontology ID (MONDO)
disease	string	disease label
classification	string	see below for possible values
classificationDate	string	yyyy-MM-dd

classification

no reported evidence
disputed
limited
moderate
definitive
strong
refuted

Overview​

Conventions​

JSON Layout​

info

Parsing​

info

Header​

Data Source​

Genome Assemblies​

Positions​

ClinGen​

1000 Genomes (SV)​

MITOMAP (SV)​

Samples​

Empty Samples

Variants​

Reference Minor Alleles

Flagging Decomposed & Recomposed Variants

Transcripts​

PolyPhen​

SIFT​

Amino Acid Conservation​

Gene Fusions​

Fusion​

Regulatory Regions​

Regulatory Types​

Regulatory Consequences​

ClinVar​

1000 Genomes​

gnomAD​

dbSNP​

MITOMAP​

Primate AI​

REVEL​

Splice AI​

TOPMed​

Genes​

OMIM​

Phenotype​

Mapping​

Inheritance​

Comments​

gnomAD LoF Gene Metrics​

ClinGen Disease Validity​

Overview

Conventions

JSON Layout

Parsing

Header

Data Source

Genome Assemblies

Positions

ClinGen

1000 Genomes (SV)

MITOMAP (SV)

Samples

Variants

Transcripts

PolyPhen

SIFT

Amino Acid Conservation

Gene Fusions

Fusion

Regulatory Regions

Regulatory Types

Regulatory Consequences

ClinVar

1000 Genomes

gnomAD

dbSNP

MITOMAP

Primate AI

REVEL

Splice AI

TOPMed

Genes

OMIM

Phenotype

Mapping

Inheritance

Comments

gnomAD LoF Gene Metrics

ClinGen Disease Validity