ClinVar Miner

List of variants reported as pathogenic for papillary adenocarcinoma by OMIM

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_001079668.3(NKX2-1):c.1106C>T (p.Ala369Val) rs537209983 0.00009
NM_000245.4(MET):c.3281A>G (p.His1094Arg) rs121913243 0.00001
NM_000051.4(ATM):c.8671+2_8671+3insTA rs2137087134
NM_000245.4(MET):c.3392T>C (p.Met1131Thr) rs121913668
NM_000245.4(MET):c.3562G>T (p.Val1188Leu) rs121913669
NM_000245.4(MET):c.3583C>G (p.Leu1195Val) rs121913673
NM_000245.4(MET):c.3658G>A (p.Val1220Ile) rs121913670
NM_000245.4(MET):c.3682G>A (p.Asp1228Asn) rs121913671
NM_000245.4(MET):c.3689A>G (p.Tyr1230Cys) rs121913246
NM_000551.4(VHL):c.548C>A (p.Ser183Ter) rs5030823
NM_004333.6(BRAF):c.1799T>A (p.Val600Glu) rs113488022

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