ClinVar for Gene (Select 79807) - ClinVar

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Links from Gene

Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3283013	NM_001370181.1(GSTCD):c.770G>A (p.Arg257Lys)	GSTCD (R170K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283012	NM_001370181.1(GSTCD):c.1259G>A (p.Arg420Gln)	GSTCD, GSTCD-AS1 (R420Q +1 more)	Single nucleotide variant (missense variant)	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 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 3062772	GRCh37/hg19 4q23-25(chr4:100172302-107880077)x1	ADH1A, ADH1B +34 more	Copy number loss	not specified	GPathogenic
Select item 3062767	GRCh37/hg19 4q24-35.2(chr4:101203509-190957473)x3	AADAT, ABCE1 +286 more	Copy number gain	not specified	GPathogenic
Select item 3062757	GRCh37/hg19 4q23-24(chr4:99355670-107274288)x1	ADH1A, ADH1B +39 more	Copy number loss	not specified	GPathogenic
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	CAMK2D, GIMD1 +537 more	Copy number gain	not provided	GPathogenic
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 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 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 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 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 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 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 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 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 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 2460420	NM_001370181.1(GSTCD):c.1874A>G (p.Asn625Ser)	GSTCD (N538S +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 2445492	NC_000004.11:g.(?_101947022)_(107268849_?)dup	SLC39A8, TBCK +19 more	Duplication	not provided	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 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 2319971	NM_001370181.1(GSTCD):c.143T>C (p.Ile48Thr)	GSTCD (I48T)	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 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 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 1527114	GRCh37/hg19 4q24-31.21(chr4:104715235-145252595)	ABHD18, ADAD1 +123 more	Copy number gain	not specified	GPathogenic
Select item 1340302	GRCh37/hg19 4q22.3-25(chr4:95490755-109977216)x3	ADH1A, ADH1B +55 more	Copy number gain	not provided	GLikely pathogenic
Select item 1340288	GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	AASDH, ABCG2 +359 more	Copy number gain	not provided	GPathogenic
Select item 686613	GRCh37/hg19 4q24(chr4:106262887-106663541)x3	ARHGEF38, GSTCD +2 more	Copy number gain	not provided	GUncertain significance
Select item 562954	GRCh37/hg19 4q24(chr4:106631903-106769321)x1	GSTCD	Copy number loss	not provided	GUncertain significance
Select item 562953	GRCh37/hg19 4q24-25(chr4:106582279-108557118)x1	NPNT, DKK2 +7 more	Copy number loss	not provided	GUncertain significance
Select item 562952	GRCh37/hg19 4q24(chr4:106507186-106882078)x3	NPNT, INTS12 +2 more	Copy number gain	not provided	GUncertain significance
Select item 443483	GRCh37/hg19 4q22.1-35.2(chr4:93071152-190957473)x3	AADAT, ABCE1 +314 more	Copy number gain	See cases	GPathogenic
Select item 441728	GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)	AADAT, AASDH +745 more	Copy number gain	See cases	GPathogenic
Select item 441727	GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3	MRPL1, MSANTD1 +745 more	Copy number gain	See cases	GPathogenic
Select item 394609	GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3	H2AZ1, HADH +744 more	Copy number gain	See cases	GPathogenic
Select item 58034	GRCh38/hg38 4q24-25(chr4:105778347-110206873)x3	AIMP1, CASP6 +106 more	Copy number gain	See cases	GPathogenic
Select item 58033	GRCh38/hg38 4q22.3-28.3(chr4:96092893-136410207)x3	LOC129993082, LOC129993083 +661 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 41