ClinVar Miner

List of variants in gene MET reported as likely pathogenic for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_001127500.3(MET):c.3334C>T (p.His1112Tyr) rs121913244
NM_001127500.3(MET):c.3335A>G (p.His1112Arg) rs121913243
NM_001127500.3(MET):c.3742T>C (p.Tyr1248His) rs121913247
NM_001127500.3(MET):c.3743A>G (p.Tyr1248Cys) rs121913246
NM_001127500.3(MET):c.3803T>C (p.Met1268Thr) rs121913245

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