"Ambry Genetics"[submitter] AND "ADH7"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2386387	NM_000673.7(ADH7):c.1118C>A (p.Thr373Lys)	ADH7 (T393K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392627	NM_000673.7(ADH7):c.977A>G (p.Asp326Gly)	ADH7 (D326G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550705	NM_000673.7(ADH7):c.934C>T (p.Arg312Cys)	ADH7 (R312C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408596	NM_000673.7(ADH7):c.893C>T (p.Ala298Val)	ADH7 (A318V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089281	NM_000673.7(ADH7):c.889T>C (p.Ser297Pro)	ADH7 (S297P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089278	NM_000673.7(ADH7):c.884C>A (p.Pro295His)	ADH7 (P315H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399347	NM_000673.7(ADH7):c.874G>A (p.Val292Ile)	ADH7 (V292I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089273	NM_000673.7(ADH7):c.868G>A (p.Val290Met)	ADH7 (V290M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089271	NM_000673.7(ADH7):c.832G>T (p.Ala278Ser)	ADH7 (A278S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089266	NM_000673.7(ADH7):c.812A>G (p.His271Arg)	ADH7 (H271R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2559749	NM_000673.7(ADH7):c.771G>A (p.Met257Ile)	ADH7 (M277I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089258	NM_000673.7(ADH7):c.763T>C (p.Ser255Pro)	ADH7 (S275P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089256	NM_000673.7(ADH7):c.659T>A (p.Ile220Asn)	ADH7 (I240N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359166	NM_000673.7(ADH7):c.586G>A (p.Val196Ile)	ADH7 (V196I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484167	NM_000673.7(ADH7):c.521G>A (p.Cys174Tyr)	ADH7 (C174Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089241	NM_000673.7(ADH7):c.505G>C (p.Val169Leu)	ADH7 (V189L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089233	NM_000673.7(ADH7):c.479T>C (p.Ile160Thr)	ADH7 (I160T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546767	NM_000673.7(ADH7):c.476A>G (p.Lys159Arg)	ADH7 (K159R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538735	NM_000673.7(ADH7):c.401G>A (p.Gly134Asp)	ADH7 (G154D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089209	NM_000673.7(ADH7):c.338T>A (p.Ile113Asn)	ADH7 (I133N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406068	NM_000673.7(ADH7):c.313C>T (p.Arg105Cys)	ADH7 (R125C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241596	NM_000673.7(ADH7):c.221T>A (p.Val74Glu)	ADH7 (V94E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264900	NM_000673.7(ADH7):c.207G>C (p.Glu69Asp)	ADH7 (E69D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294071	NM_000673.7(ADH7):c.196G>A (p.Val66Met)	ADH7 (V86M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615820	NM_000673.7(ADH7):c.169A>G (p.Thr57Ala)	ADH7 (T57A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2301917	NM_000673.7(ADH7):c.83A>C (p.Glu28Ala)	ADH7 (E48A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539923	NM_000673.7(ADH7):c.58C>G (p.Gln20Glu)	ADH7 (Q20E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27