"Laboratory of Otorhinolaryngology, Head and Neck Surgery, Seoul Natio - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1895419	NM_138691.3(TMC1):c.1256T>C (p.Phe419Ser)	TMC1 (F419S)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 36	GUncertain significance
Select item 1895420	NM_138691.3(TMC1):c.1444T>C (p.Trp482Arg)	TMC1 (W482R)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 36	GUncertain significance