"Ambry Genetics"[submitter] AND "GSTZ1"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3103005	NM_145870.3(GSTZ1):c.38G>A (p.Arg13Gln)	GSTZ1 (R14Q +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2280359	NM_145870.3(GSTZ1):c.65T>C (p.Ile22Thr)	GSTZ1 (I23T +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2384672	NM_145870.3(GSTZ1):c.98C>T (p.Thr33Met)	GSTZ1 (T34M +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2216507	NM_145870.3(GSTZ1):c.128G>T (p.Gly43Val)	GSTZ1 (G43V +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3103001	NM_145870.3(GSTZ1):c.174G>T (p.Gln58His)	GSTZ1 (Q58H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240816	NM_145870.3(GSTZ1):c.220G>A (p.Ala74Thr)	GSTZ1 (A19T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103002	NM_145870.3(GSTZ1):c.246G>A (p.Met82Ile)	GSTZ1 (M82I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103003	NM_145870.3(GSTZ1):c.257C>T (p.Pro86Leu)	GSTZ1 (P31L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2264874	NM_145870.3(GSTZ1):c.299G>A (p.Arg100His)	GSTZ1 (R101H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527218	NM_145870.3(GSTZ1):c.319G>A (p.Ala107Thr)	GSTZ1 (A107T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273491	NM_145870.3(GSTZ1):c.400G>A (p.Ala134Thr)	GSTZ1 (A134T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283032	NM_145870.3(GSTZ1):c.467G>A (p.Gly156Glu)	GSTZ1, LOC126862005 (G156E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275669	NM_145870.3(GSTZ1):c.472G>A (p.Glu158Lys)	GSTZ1, LOC126862005 (E116K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103006	NM_145870.3(GSTZ1):c.532G>T (p.Val178Leu)	GSTZ1 (V179L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103007	NM_145870.3(GSTZ1):c.599A>C (p.Gln200Pro)	GSTZ1 (Q200P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance