ClinVar Miner

List of variants in gene TMC1 reported as uncertain significance for not specified

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Total variants: 33
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HGVS dbSNP
NM_138691.2(TMC1):c.1018A>G (p.Met340Val) rs771281791
NM_138691.2(TMC1):c.1022A>C (p.Asn341Thr) rs727504568
NM_138691.2(TMC1):c.1030-3C>T rs370872111
NM_138691.2(TMC1):c.1189G>A (p.Asp397Asn) rs185702148
NM_138691.2(TMC1):c.1224+5G>A rs397517835
NM_138691.2(TMC1):c.1265C>A (p.Thr422Lys) rs868082421
NM_138691.2(TMC1):c.1369T>C (p.Phe457Leu) rs397517836
NM_138691.2(TMC1):c.1404+4A>G rs727503484
NM_138691.2(TMC1):c.141T>A (p.Asp47Glu) rs140388347
NM_138691.2(TMC1):c.145A>C (p.Ile49Leu) rs149947445
NM_138691.2(TMC1):c.1532C>A (p.Pro511His) rs727503483
NM_138691.2(TMC1):c.1567-14T>G rs727503485
NM_138691.2(TMC1):c.1705A>G (p.Thr569Ala) rs148971770
NM_138691.2(TMC1):c.1796G>A (p.Gly599Asp) rs727503486
NM_138691.2(TMC1):c.1902C>G (p.Asn634Lys) rs767285617
NM_138691.2(TMC1):c.1988A>G (p.Asp663Gly) rs397517837
NM_138691.2(TMC1):c.1992T>G (p.Cys664Trp) rs727503487
NM_138691.2(TMC1):c.2044G>C (p.Glu682Gln) rs199819595
NM_138691.2(TMC1):c.2068G>A (p.Ala690Thr) rs397517838
NM_138691.2(TMC1):c.2144A>T (p.Tyr715Phe) rs41310067
NM_138691.2(TMC1):c.2230C>T (p.Arg744Ter) rs150738413
NM_138691.2(TMC1):c.339G>A (p.Met113Ile) rs397517840
NM_138691.2(TMC1):c.403G>A (p.Gly135Arg) rs397517841
NM_138691.2(TMC1):c.448G>A (p.Ala150Thr) rs534560340
NM_138691.2(TMC1):c.472C>T (p.Arg158Cys) rs200841002
NM_138691.2(TMC1):c.532G>A
NM_138691.2(TMC1):c.543T>G
NM_138691.2(TMC1):c.557C>G (p.Ala186Gly) rs727504470
NM_138691.2(TMC1):c.637C>T (p.Pro213Ser) rs745569653
NM_138691.2(TMC1):c.791G>C (p.Arg264Pro) rs147147941
NM_138691.2(TMC1):c.7C>A (p.Pro3Thr) rs569626109
NM_138691.2(TMC1):c.841G>T (p.Gly281Trp) rs397517842
NM_138691.2(TMC1):c.884+2dup rs876658020

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