ClinVar for Gene (Select 414201) - ClinVar - NCBI

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Links from Gene

Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3195124	NM_006973.3(ZNF32):c.484G>A (p.Glu162Lys)	ZNF32, ZNF32-AS1 +1 more (E137K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195123	NM_006973.3(ZNF32):c.346G>A (p.Ala116Thr)	ZNF32, ZNF32-AS1 +1 more (A116T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195122	NM_006973.3(ZNF32):c.318G>T (p.Glu106Asp)	ZNF32, ZNF32-AS1 +1 more (E81D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640420	NM_006973.3(ZNF32):c.622A>G (p.Ile208Val)	ZNF32, ZNF32-AS1 +1 more (I183V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2623044	NM_006973.3(ZNF32):c.669G>T (p.Arg223Ser)	ZNF32, ZNF32-AS1 +1 more (R227S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619969	NM_006973.3(ZNF32):c.623T>C (p.Ile208Thr)	ZNF32, ZNF32-AS1 +1 more (I183T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546332	NM_006973.3(ZNF32):c.604G>A (p.Gly202Arg)	ZNF32, ZNF32-AS1 +1 more (G202R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381513	NM_006973.3(ZNF32):c.221A>G (p.Gln74Arg)	ZNF32, ZNF32-AS1 +1 more (Q78R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369630	NM_006973.3(ZNF32):c.454G>A (p.Glu152Lys)	ZNF32, ZNF32-AS1 +1 more (E127K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363242	NM_006973.3(ZNF32):c.89A>G (p.His30Arg)	ZNF32, ZNF32-AS1 +1 more (H34R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316598	NM_006973.3(ZNF32):c.259C>T (p.Arg87Trp)	ZNF32, ZNF32-AS1 +1 more (R91W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217027	NM_006973.3(ZNF32):c.278C>T (p.Thr93Met)	ZNF32, ZNF32-AS1 +1 more (T93M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207596	NM_006973.3(ZNF32):c.260G>A (p.Arg87Gln)	ZNF32, ZNF32-AS1 +1 more (R91Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 154900	GRCh38/hg38 10q11.21-21.3(chr10:42112187-67400675)x3	A1CF, ADO +561 more	Copy number gain	See cases	GPathogenic
Select item 152998	GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	AGAP4, AGAP9 +1221 more	Copy number gain	See cases	GBenign
Select item 145481	GRCh38/hg38 10q11.21-22.2(chr10:42685306-73715908)x3	A1CF, ADAMTS14 +902 more	Copy number gain	See cases	GPathogenic
Select item 145479	GRCh38/hg38 10q11.21-11.23(chr10:42395201-50877059)x3	LOC130003758, LOC130003759 +309 more	Copy number gain	See cases	GPathogenic
Select item 144977	GRCh38/hg38 10q11.21-21.1(chr10:42884294-52265317)x3	FAM170B, FAM170B-AS1 +306 more	Copy number gain	See cases	GPathogenic