ClinVar Miner

List of variants in gene KIT reported as uncertain significance for connective tissue neoplasm

Included ClinVar conditions (122):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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NM_000222.2(KIT):c.1553C>T (p.Pro518Leu) rs569408054
NM_000222.2(KIT):c.200C>G (p.Thr67Ser) rs144933028
NM_000222.2(KIT):c.2057G>A (p.Arg686His) rs143772138
NM_000222.2(KIT):c.2104C>G (p.Leu702Val) rs768847037
NM_000222.2(KIT):c.2294A>G (p.Asp765Gly) rs1060502545
NM_000222.2(KIT):c.2836C>T (p.Arg946Ter) rs139000082
NM_000222.2(KIT):c.2863G>T (p.Val955Leu) rs1060502568
NM_000222.2(KIT):c.2881G>A (p.Gly961Ser) rs773828910
NM_000222.2(KIT):c.2887A>G (p.Thr963Ala) rs773709702
NM_000222.2(KIT):c.2900C>G (p.Ser967Cys) rs1232060384
NM_000222.2(KIT):c.302A>G (p.His101Arg) rs1274601103

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