"Ambry Genetics"[submitter] AND "ADH6"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3089091	NM_001102470.2(ADH6):c.1079T>C (p.Val360Ala)	ADH6, LOC100507053 (V360A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3089088	NM_001102470.2(ADH6):c.1076C>G (p.Ala359Gly)	ADH6, LOC100507053 (A359G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599871	NM_001102470.2(ADH6):c.1054A>T (p.Asn352Tyr)	ADH6, LOC100507053 (N352Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218691	NM_001102470.2(ADH6):c.1010T>C (p.Met337Thr)	ADH6, LOC100507053 (M337T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2478023	NM_001102470.2(ADH6):c.982C>T (p.His328Tyr)	ADH6, LOC100507053 (H328Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2564124	NM_001102470.2(ADH6):c.937C>T (p.Arg313Cys)	ADH6, LOC100507053 (R313C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2388508	NM_001102470.2(ADH6):c.841G>A (p.Ala281Thr)	ADH6, LOC100507053 (A281T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3089130	NM_001102470.2(ADH6):c.814A>C (p.Asn272His)	ADH6, LOC100507053 (N272H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488566	NM_001102470.2(ADH6):c.700C>A (p.Gln234Lys)	ADH6, LOC100507053 (Q234K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2315442	NM_001102470.2(ADH6):c.649G>A (p.Ala217Thr)	ADH6, LOC100507053 (A217T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3089113	NM_001102470.2(ADH6):c.466A>G (p.Ile156Val)	ADH6, LOC100507053 (I156V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262599	NM_001102470.2(ADH6):c.328G>A (p.Gly110Ser)	ADH6, LOC100507053 (G110S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314698	NM_001102470.2(ADH6):c.275T>C (p.Ile92Thr)	ADH6, LOC100507053 (I92T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3089104	NM_001102470.2(ADH6):c.265G>A (p.Asp89Asn)	ADH6, LOC100507053 (D89N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241964	NM_001102470.2(ADH6):c.217G>A (p.Gly73Arg)	ADH6, LOC100507053 (G73R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300138	NM_001102470.2(ADH6):c.64T>C (p.Phe22Leu)	ADH6, LOC100507053 (F22L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3089096	NM_001102470.2(ADH6):c.19G>T (p.Val7Phe)	ADH6, LOC100507053 (V7F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance