"Ambry Genetics"[submitter] AND "VMP1"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3332113	NM_030938.5(VMP1):c.52G>A (p.Glu18Lys)	VMP1 (E18K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368407	NM_030938.5(VMP1):c.165G>T (p.Gln55His)	VMP1 (Q55H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2275189	NM_030938.5(VMP1):c.485A>G (p.Tyr162Cys)	VMP1 (Y65C +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2456295	NM_030938.5(VMP1):c.529A>G (p.Thr177Ala)	VMP1 (T43A +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2356929	NM_030938.5(VMP1):c.830C>T (p.Thr277Met)	VMP1 (T124M +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328493	NM_030938.5(VMP1):c.1066G>T (p.Gly356Cys)	LOC114827848, VMP1 (G164C +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188701	NM_030938.5(VMP1):c.1094C>T (p.Ser365Phe)	VMP1 (S268F +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383200	NM_030938.5(VMP1):c.1117G>A (p.Val373Ile)	VMP1 (V317I +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523541	NM_030938.5(VMP1):c.1141C>G (p.Leu381Val)	VMP1 (L344V +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527924	NM_030938.5(VMP1):c.1147A>C (p.Ile383Leu)	VMP1 (I230L +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance