ClinVar Miner

List of variants in gene TMC1 studied for Nonsyndromic Hearing Loss, Dominant

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Total variants: 32
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HGVS dbSNP
NM_138691.2(TMC1):c.*106G>C rs79830675
NM_138691.2(TMC1):c.*156T>C rs545955592
NM_138691.2(TMC1):c.*183A>G rs71507808
NM_138691.2(TMC1):c.*28A>C rs151157872
NM_138691.2(TMC1):c.*51G>A rs771430357
NM_138691.2(TMC1):c.*93C>T rs184207177
NM_138691.2(TMC1):c.-124T>C rs533837914
NM_138691.2(TMC1):c.-219A>G rs7026304
NM_138691.2(TMC1):c.-220C>T rs1057515621
NM_138691.2(TMC1):c.-252C>T rs541857536
NM_138691.2(TMC1):c.-329C>A rs7856724
NM_138691.2(TMC1):c.-350C>T rs1022291966
NM_138691.2(TMC1):c.-468G>A rs7022441
NM_138691.2(TMC1):c.-540C>T rs112220638
NM_138691.2(TMC1):c.1457T>C (p.Met486Thr) rs17058153
NM_138691.2(TMC1):c.1584A>G (p.Thr528=) rs762248733
NM_138691.2(TMC1):c.1608C>T (p.Tyr536=) rs552170649
NM_138691.2(TMC1):c.1609G>A (p.Val537Ile) rs150206751
NM_138691.2(TMC1):c.1713C>T (p.Phe571=) rs34532421
NM_138691.2(TMC1):c.1763+3A>G rs370898981
NM_138691.2(TMC1):c.2204A>C (p.Lys735Thr) rs1057515624
NM_138691.2(TMC1):c.2261-15_2261-14del rs777589679
NM_138691.2(TMC1):c.237-5T>A rs1057515622
NM_138691.2(TMC1):c.238_240GAA[3] (p.Glu83del) rs376040866
NM_138691.2(TMC1):c.241G>A (p.Glu81Lys) rs1796993
NM_138691.2(TMC1):c.421C>T (p.Arg141Trp) rs11143384
NM_138691.2(TMC1):c.45C>T (p.Asp15=) rs2589615
NM_138691.2(TMC1):c.473G>A (p.Arg158His) rs148340276
NM_138691.2(TMC1):c.703G>T (p.Ala235Ser) rs200831684
NM_138691.2(TMC1):c.795A>C (p.Thr265=) rs140398130
NM_138691.2(TMC1):c.910G>A (p.Gly304Arg) rs1008565149
NM_138691.2(TMC1):c.924C>G (p.Asp308Glu) rs113342704

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