ClinVar Miner

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

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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_000222.3(KIT):c.2586G>C (p.Leu862=) rs3733542 0.16755
NM_000222.3(KIT):c.*1704G>T rs8022 0.16223
NM_000222.3(KIT):c.*149C>T rs2213181 0.11143
NM_000222.3(KIT):c.*217G>A rs17084733 0.10193
NM_000222.3(KIT):c.1621A>C (p.Met541Leu) rs3822214 0.07727
NM_000222.3(KIT):c.2142-36A>G rs17084713 0.02490
NM_000222.3(KIT):c.1638A>G (p.Lys546=) rs55986963 0.02258
NM_000222.3(KIT):c.2394C>T (p.Ile798=) rs55789615 0.02125
NM_000222.3(KIT):c.2847C>T (p.Pro949=) rs56288823 0.01843
NM_000222.3(KIT):c.67+4G>A rs72550820 0.00969
NM_000222.3(KIT):c.1119C>T (p.Tyr373=) rs72549293 0.00964
NM_000222.3(KIT):c.1794A>T (p.Gly598=) rs72549292 0.00952
NM_000222.3(KIT):c.*66T>G rs112972811 0.00939
NM_000222.3(KIT):c.*1241G>A rs114377961 0.00931
NM_000222.3(KIT):c.*1524A>G rs17084736 0.00815
NM_000222.3(KIT):c.532G>A (p.Ala178Thr) rs115585711 0.00342
NM_000222.3(KIT):c.1383A>G (p.Thr461=) rs151016327 0.00324
NM_000222.3(KIT):c.*352A>G rs149336515 0.00319
NM_000222.3(KIT):c.1120G>A (p.Val374Ile) rs73137716 0.00218
NM_000222.3(KIT):c.1199A>G (p.Asn400Ser) rs72549294 0.00215
NM_000222.3(KIT):c.2361T>C (p.Asn787=) rs140912933 0.00207
NM_000222.3(KIT):c.2622G>A (p.Pro874=) rs55817813 0.00188
NM_000222.3(KIT):c.123A>T (p.Pro41=) rs72549300 0.00182
NM_000222.3(KIT):c.2805T>A (p.Ile935=) rs72549296 0.00176
NM_000222.3(KIT):c.821C>T (p.Thr274Met) rs138585275 0.00035
NM_000222.3(KIT):c.67+12C>T rs374618962 0.00031
NM_000222.3(KIT):c.925+9C>T rs201405378 0.00029
NM_000222.3(KIT):c.251C>T (p.Thr84Met) rs201872586 0.00019
NM_000222.3(KIT):c.1694G>T (p.Gly565Val) rs200945282 0.00009
NM_000222.3(KIT):c.2234-8C>T rs199817515 0.00009
NM_000222.3(KIT):c.2262C>T (p.Pro754=) rs200112919 0.00007
NM_000222.3(KIT):c.372G>A (p.Leu124=) rs775690281 0.00006
NM_000222.3(KIT):c.1290A>G (p.Ala430=) rs55966164 0.00004
NM_000222.3(KIT):c.735G>A (p.Thr245=) rs150150449 0.00003
NM_000222.3(KIT):c.1137A>G (p.Leu379=) rs773723931 0.00002
NM_000222.3(KIT):c.1115+16del rs761590943
NM_000222.3(KIT):c.1232-8dup
NM_000222.3(KIT):c.1346+17del rs2109761509
NM_000222.3(KIT):c.1347-12del
NM_000222.3(KIT):c.1991-16del
NM_000222.3(KIT):c.252G>A (p.Thr84=) rs56411694
NM_000222.3(KIT):c.252G>T (p.Thr84=) rs56411694
NM_000222.3(KIT):c.337+14T>G
NM_000222.3(KIT):c.338-17del
NM_000222.3(KIT):c.620-9del
NM_000222.3(KIT):c.620-9dup

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