ClinVar Miner

List of variants in gene TMC1 reported as uncertain significance for auditory system disease

Included ClinVar conditions (549):
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Gene type:
ClinVar version:
Total variants: 56
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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.-220C>T rs1057515621
NM_138691.2(TMC1):c.-252C>T rs541857536
NM_138691.2(TMC1):c.-350C>T rs1022291966
NM_138691.2(TMC1):c.1114G>A (p.Val372Met) rs367924428
NM_138691.2(TMC1):c.1141T>A (p.Tyr381Asn) rs749491943
NM_138691.2(TMC1):c.1263A>G (p.Pro421=) rs139985214
NM_138691.2(TMC1):c.1333C>T (p.Arg445Cys) rs372710475
NM_138691.2(TMC1):c.145A>C (p.Ile49Leu) rs149947445
NM_138691.2(TMC1):c.1567-14T>G rs727503485
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.2070G>A (p.Ala690=) rs145757452
NM_138691.2(TMC1):c.2144A>T (p.Tyr715Phe) rs41310067
NM_138691.2(TMC1):c.2177C>T (p.Ala726Val) rs573874378
NM_138691.2(TMC1):c.2204A>C (p.Lys735Thr) rs1057515624
NM_138691.2(TMC1):c.2275C>T (p.Arg759Cys)
NM_138691.2(TMC1):c.237-5T>A rs1057515622
NM_138691.2(TMC1):c.339G>A (p.Met113Ile) rs397517840
NM_138691.2(TMC1):c.373A>C (p.Lys125Gln) rs377607548
NM_138691.2(TMC1):c.421C>T (p.Arg141Trp) rs11143384
NM_138691.2(TMC1):c.473G>A (p.Arg158His) rs148340276
NM_138691.2(TMC1):c.596A>T (p.Asn199Ile) rs756960425
NM_138691.2(TMC1):c.624C>A (p.Ser208Arg) rs781747541
NM_138691.2(TMC1):c.703G>T (p.Ala235Ser) rs200831684
NM_138691.2(TMC1):c.760G>A (p.Val254Ile) rs111033497
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
NM_138691.2(TMC1):c.938T>C (p.Phe313Ser) rs1060499599
NM_138691.3(TMC1):c.*10T>C
NM_138691.3(TMC1):c.*26G>C
NM_138691.3(TMC1):c.*302A>G
NM_138691.3(TMC1):c.-275G>A
NM_138691.3(TMC1):c.-295A>T
NM_138691.3(TMC1):c.-385G>A
NM_138691.3(TMC1):c.-442T>G
NM_138691.3(TMC1):c.-481T>C
NM_138691.3(TMC1):c.1201C>A (p.Leu401Ile)
NM_138691.3(TMC1):c.1417A>C (p.Lys473Gln)
NM_138691.3(TMC1):c.1594G>A (p.Val532Ile)
NM_138691.3(TMC1):c.1660A>T (p.Asn554Tyr)
NM_138691.3(TMC1):c.1708G>A (p.Glu570Lys) rs369890353
NM_138691.3(TMC1):c.2011A>G (p.Asn671Asp)
NM_138691.3(TMC1):c.2163G>C (p.Lys721Asn) rs1588105861
NM_138691.3(TMC1):c.2245G>T (p.Ala749Ser)
NM_138691.3(TMC1):c.2276G>A (p.Arg759His)
NM_138691.3(TMC1):c.46G>A (p.Glu16Lys)
NM_138691.3(TMC1):c.976G>A (p.Gly326Ser)

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