ClinVar Miner

List of variants in gene KIT reported as benign for Gastrointestinal stroma tumor

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Total variants: 23
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HGVS dbSNP
NM_000222.2(KIT):c.1119C>T (p.Tyr373=) rs72549293
NM_000222.2(KIT):c.1120G>A (p.Val374Ile) rs73137716
NM_000222.2(KIT):c.1137A>G (p.Leu379=) rs773723931
NM_000222.2(KIT):c.1199A>G (p.Asn400Ser) rs72549294
NM_000222.2(KIT):c.123A>T (p.Pro41=) rs72549300
NM_000222.2(KIT):c.1290A>G (p.Ala430=) rs55966164
NM_000222.2(KIT):c.1383A>G (p.Thr461=) rs151016327
NM_000222.2(KIT):c.1638A>G (p.Lys546=) rs55986963
NM_000222.2(KIT):c.1794A>T (p.Gly598=) rs72549292
NM_000222.2(KIT):c.2234-8C>T rs199817515
NM_000222.2(KIT):c.2262C>T (p.Pro754=) rs200112919
NM_000222.2(KIT):c.2361T>C (p.Asn787=) rs140912933
NM_000222.2(KIT):c.2394C>T (p.Ile798=) rs55789615
NM_000222.2(KIT):c.252G>A (p.Thr84=) rs56411694
NM_000222.2(KIT):c.252G>T (p.Thr84=) rs56411694
NM_000222.2(KIT):c.2622G>A (p.Pro874=) rs55817813
NM_000222.2(KIT):c.2805T>A (p.Ile935=) rs72549296
NM_000222.2(KIT):c.2847C>T (p.Pro949=) rs56288823
NM_000222.2(KIT):c.372G>A (p.Leu124=) rs775690281
NM_000222.2(KIT):c.532G>A (p.Ala178Thr) rs115585711
NM_000222.2(KIT):c.67+4G>A rs72550820
NM_000222.2(KIT):c.735G>A (p.Thr245=) rs150150449
NM_000222.2(KIT):c.821C>T (p.Thr274Met) rs138585275

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