List of variants in gene TMC1 reported as pathogenic for autosomal dominant nonsyndromic hearing loss

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_138691.3(TMC1):c.1534C>T (p.Arg512Ter)	rs200171616	0.00031
NM_138691.3(TMC1):c.100C>T (p.Arg34Ter)	rs121908073	0.00006
NM_138691.3(TMC1):c.1165C>T (p.Arg389Ter)	rs151001642	0.00006
NM_138691.3(TMC1):c.236+1G>A	rs775428246	0.00003
NM_138691.3(TMC1):c.1939T>C (p.Ser647Pro)	rs138527651	0.00002
NM_138691.3(TMC1):c.821C>T (p.Pro274Leu)	rs755694066	0.00002
NM_138691.3(TMC1):c.1810C>T (p.Arg604Ter)	rs777777359	0.00001
NM_138691.3(TMC1):c.1253T>A (p.Met418Lys)	rs786201027
NM_138691.3(TMC1):c.150del (p.Asn50fs)	rs2132189585
NM_138691.3(TMC1):c.15dup (p.Val6fs)	rs878853229
NM_138691.3(TMC1):c.1627G>A (p.Asp543Asn)
NM_138691.3(TMC1):c.1714G>A (p.Asp572Asn)	rs121908072
NM_138691.3(TMC1):c.1714G>C (p.Asp572His)	rs121908072
NM_138691.3(TMC1):c.1764G>A (p.Trp588Ter)
NM_138691.3(TMC1):c.535+1G>C

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