mitomap-small-variants-json
"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 |