C1847626[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 4103	NM_138691.3(TMC1):c.100C>T (p.Arg34Ter)	TMC1 (R34*)	Single nucleotide variant (nonsense)	Rare genetic deafness +3 more	GPathogenic
Select item 47871	NM_138691.3(TMC1):c.339G>A (p.Met113Ile)	TMC1 (M113I)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 1306523	NM_138691.3(TMC1):c.968A>G (p.Tyr323Cys)	TMC1 (Y323C)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance

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