"Ambry Genetics"[submitter] AND "VDAC2"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2312233	NM_001391963.1(VDAC2):c.106G>A (p.Gly36Arg)	VDAC2 (G36R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557309	NM_001391963.1(VDAC2):c.134A>G (p.Lys45Arg)	VDAC2 (K60R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525479	NM_001391963.1(VDAC2):c.141C>G (p.Cys47Trp)	VDAC2 (C62W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188418	NM_001391963.1(VDAC2):c.238C>G (p.Leu80Val)	VDAC2 (L80V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615934	NM_001391963.1(VDAC2):c.248C>T (p.Thr83Ile)	VDAC2 (T83I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241313	NM_001391963.1(VDAC2):c.332A>T (p.Asp111Val)	VDAC2 (D111V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188419	NM_001391963.1(VDAC2):c.496A>C (p.Met166Leu)	VDAC2 (M127L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188420	NM_001391963.1(VDAC2):c.517T>G (p.Ser173Ala)	VDAC2 (S188A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383967	NM_001391963.1(VDAC2):c.578C>T (p.Thr193Ile)	VDAC2 (T154I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188421	NM_001391963.1(VDAC2):c.796G>A (p.Val266Met)	VDAC2 (V266M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188422	NM_001391963.1(VDAC2):c.808C>T (p.Leu270Phe)	VDAC2 (L285F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492918	NM_001391963.1(VDAC2):c.835A>G (p.Ile279Val)	VDAC2 (I240V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305333	NM_001391963.1(VDAC2):c.841G>A (p.Ala281Thr)	VDAC2 (A242T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance