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

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2319971	NM_001370181.1(GSTCD):c.143T>C (p.Ile48Thr)	GSTCD (I48T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515382	NM_001370181.1(GSTCD):c.176A>G (p.Asp59Gly)	GSTCD (D59G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102968	NM_001370181.1(GSTCD):c.274G>A (p.Ala92Thr)	GSTCD (A92T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512410	NM_001370181.1(GSTCD):c.296A>G (p.Asn99Ser)	GSTCD (N99S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102969	NM_001370181.1(GSTCD):c.360C>A (p.Asp120Glu)	GSTCD (D120E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2375697	NM_001370181.1(GSTCD):c.373G>C (p.Glu125Gln)	GSTCD (E125Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351021	NM_001370181.1(GSTCD):c.511A>G (p.Thr171Ala)	GSTCD (T171A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2272619	NM_001370181.1(GSTCD):c.557C>T (p.Pro186Leu)	GSTCD (P186L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588648	NM_001370181.1(GSTCD):c.565G>A (p.Val189Met)	GSTCD (V102M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472100	NM_001370181.1(GSTCD):c.586C>T (p.Arg196Cys)	GSTCD (R109C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493459	NM_001370181.1(GSTCD):c.599T>G (p.Leu200Arg)	GSTCD (L113R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589149	NM_001370181.1(GSTCD):c.712G>A (p.Glu238Lys)	GSTCD (E151K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595596	NM_001370181.1(GSTCD):c.814C>G (p.Pro272Ala)	GSTCD (P185A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467120	NM_001370181.1(GSTCD):c.1088A>G (p.Glu363Gly)	GSTCD (E276G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598392	NM_001370181.1(GSTCD):c.1167G>A (p.Met389Ile)	GSTCD (M389I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247687	NM_001370181.1(GSTCD):c.1390C>T (p.Pro464Ser)	GSTCD, GSTCD-AS1 (P377S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312289	NM_001370181.1(GSTCD):c.1453A>G (p.Ser485Gly)	GSTCD, GSTCD-AS1 (S485G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528384	NM_001370181.1(GSTCD):c.1547G>T (p.Cys516Phe)	GSTCD (C429F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455303	NM_001370181.1(GSTCD):c.1646A>G (p.Lys549Arg)	GSTCD (K462R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400079	NM_001370181.1(GSTCD):c.1652A>G (p.Asn551Ser)	GSTCD (N464S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460420	NM_001370181.1(GSTCD):c.1874A>G (p.Asn625Ser)	GSTCD (N538S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 21