ClinVar Miner

List of variants studied for Gastrointestinal stromal tumor by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_006206.6(PDGFRA):c.661C>T (p.Leu221Phe) rs139913632 0.00307
NM_000222.3(KIT):c.200C>G (p.Thr67Ser) rs144933028 0.00045
NM_000222.3(KIT):c.1594G>A (p.Val532Ile) rs55792975 0.00028
NM_000222.3(KIT):c.101C>T (p.Pro34Leu) rs55755457 0.00010
NM_000222.3(KIT):c.2867G>A (p.Arg956Gln) rs139694927 0.00008
NM_000222.3(KIT):c.2920G>A (p.Asp974Asn) rs72549297 0.00006
NM_000222.3(KIT):c.910A>G (p.Thr304Ala) rs202052259 0.00006
NM_000222.3(KIT):c.2056C>T (p.Arg686Cys) rs148771698 0.00005
NM_000222.3(KIT):c.391G>A (p.Asp131Asn) rs1044091916 0.00004
NM_000222.3(KIT):c.1336A>G (p.Thr446Ala) rs1351743650 0.00002
NM_000222.3(KIT):c.2621C>T (p.Pro874Leu) rs753419764 0.00001
NM_000222.3(KIT):c.1228A>T (p.Asn410Tyr)
NM_000222.3(KIT):c.124G>A (p.Gly42Arg)
NM_000222.3(KIT):c.1412A>C (p.Lys471Thr)
NM_000222.3(KIT):c.340C>G (p.Pro114Ala) rs772836939

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