List of variants reported as pathogenic for autosomal recessive nonsyndromic hearing loss 7

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_138691.3(TMC1):c.1763+3A>G	rs370898981	0.00056
NM_138691.3(TMC1):c.100C>T (p.Arg34Ter)	rs121908073	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.1960A>G (p.Met654Val)	rs121908074	0.00002
NM_138691.3(TMC1):c.821C>T (p.Pro274Leu)	rs755694066	0.00002
NM_138691.3(TMC1):c.797T>C (p.Ile266Thr)	rs747645756	0.00001
NM_138691.2(TMC1):c.[1165C>T];[1939T>C]
NM_138691.2(TMC1):c.[1210T>C];[1939T>C]
NM_138691.2(TMC1):c.[1810C>T];[1939T>C]
NM_138691.2(TMC1):c.[1810C>T];[674C>T]
NM_138691.3(TMC1):c.1143C>G (p.Tyr381Ter)	rs757327146
NM_138691.3(TMC1):c.1184del (p.Gln395fs)	rs2118181420
NM_138691.3(TMC1):c.1220dup (p.Asn407fs)	rs1564555185
NM_138691.3(TMC1):c.1250G>A (p.Gly417Glu)
NM_138691.3(TMC1):c.1259G>A (p.Cys420Tyr)	rs1564556995
NM_138691.3(TMC1):c.150del (p.Asn50fs)	rs2132189585
NM_138691.3(TMC1):c.1532C>T (p.Pro511Leu)	rs727503483
NM_138691.3(TMC1):c.1543T>C (p.Cys515Arg)	rs121908076
NM_138691.3(TMC1):c.15dup (p.Val6fs)	rs878853229
NM_138691.3(TMC1):c.16+1G>T	rs1169090943
NM_138691.3(TMC1):c.2218G>T (p.Glu740Ter)	rs1564583413
NM_138691.3(TMC1):c.229del (p.Arg77fs)	rs878853230
NM_138691.3(TMC1):c.871del (p.Val291fs)
NM_138691.3(TMC1):c.885-2A>C	rs1564554148

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