ClinVar Miner

List of variants in gene MET reported as likely pathogenic for adenocarcinoma

Included ClinVar conditions (109):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.3281A>G (p.His1094Arg) rs121913243 0.00001
NM_000245.4(MET):c.3280C>T (p.His1094Tyr) rs121913244
NM_000245.4(MET):c.3658G>A (p.Val1220Ile) rs121913670
NM_000245.4(MET):c.3688T>C (p.Tyr1230His) rs121913247
NM_000245.4(MET):c.3689A>G (p.Tyr1230Cys) rs121913246
NM_000245.4(MET):c.3749T>C (p.Met1250Thr) rs121913245

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