ZNF641[gene] - ClinVar

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

Search results

Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	FERRY3, FGD4 +4837 more	Copy number gain	See cases	GPathogenic
Select item 2243969	NM_001172681.2(ZNF641):c.1124G>A (p.Arg375Lys)	ZNF641 (R375K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484458	NM_001172681.2(ZNF641):c.1049G>A (p.Arg350His)	ZNF641 (R350H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259017	NM_001172681.2(ZNF641):c.953A>G (p.Asn318Ser)	ZNF641 (N309S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555690	NM_001172681.2(ZNF641):c.953A>C (p.Asn318Thr)	ZNF641 (N175T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456904	NM_001172681.2(ZNF641):c.844A>G (p.Lys282Glu)	ZNF641 (K273E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197400	NM_001172681.2(ZNF641):c.793C>T (p.Leu265Phe)	ZNF641 (L256F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227548	NM_001172681.2(ZNF641):c.680C>G (p.Pro227Arg)	ZNF641 (P218R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197399	NM_001172681.2(ZNF641):c.667C>T (p.Leu223Phe)	ZNF641 (L214F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197398	NM_001172681.2(ZNF641):c.651C>G (p.Ser217Arg)	ZNF641 (S217R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2217913	NM_001172681.2(ZNF641):c.649A>C (p.Ser217Arg)	ZNF641 (S217R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2212427	NM_001172681.2(ZNF641):c.636G>C (p.Trp212Cys)	ZNF641 (W203C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354787	NM_001172681.2(ZNF641):c.626A>G (p.Asp209Gly)	ZNF641 (D200G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197397	NM_001172681.2(ZNF641):c.617C>T (p.Pro206Leu)	ZNF641 (P197L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219617	NM_001172681.2(ZNF641):c.610T>C (p.Trp204Arg)	ZNF641 (W218R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197396	NM_001172681.2(ZNF641):c.577A>T (p.Met193Leu)	ZNF641 (M193L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273988	NM_001172681.2(ZNF641):c.577A>G (p.Met193Val)	ZNF641 (M184V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197395	NM_001172681.2(ZNF641):c.560A>G (p.Glu187Gly)	ZNF641 (E187G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607339	NM_001172681.2(ZNF641):c.526G>C (p.Gly176Arg)	ZNF641 (G190R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225845	NM_001172681.2(ZNF641):c.462A>T (p.Gln154His)	ZNF641 (Q11H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458249	NM_001172681.2(ZNF641):c.176A>C (p.Gln59Pro)	ZNF641 (Q59P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259016	NM_001172681.2(ZNF641):c.89G>A (p.Gly30Glu)	ZNF641 (G30E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456527	NM_001172681.2(ZNF641):c.67G>C (p.Ala23Pro)	ZNF641 (A37P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197401	NM_001172681.2(ZNF641):c.46A>T (p.Met16Leu)	ZNF641 (M16L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526712	NM_001172681.2(ZNF641):c.-26+730G>A	ZNF641 (A3T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1710515	GRCh37/hg19 12q12-13.11(chr12:44661149-48921204)x1	AMIGO2, ANO6 +27 more	Copy number loss	not provided	GPathogenic
Select item 1527702	GRCh37/hg19 12q11-13.12(chr12:37857750-49791459)	ABCD2, ADAMTS20 +72 more	Copy number gain	not specified	GPathogenic
Select item 1048618	GRCh37/hg19 12q11-13.12(chr12:37873948-49578619)x3	PPHLN1, PRICKLE1 +66 more	Copy number gain	See cases	GLikely pathogenic
Select item 524190	NC_000012.11:g.26370251_54361538inv	BICD1, HDAC7 +212 more	Inversion	not specified	GUncertain significance
Select item 441984	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	SLC15A5, SLC16A7 +1006 more	Copy number gain	See cases	GPathogenic
Select item 441983	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	A2M, A2ML1 +1006 more	Copy number gain	See cases	GPathogenic
Select item 268075	GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	GALNT8, H2AJ +1007 more	Copy number gain	See cases	GPathogenic
Select item 221992	GRCh37/hg19 12p11.21-q13.12(chr12:31886971-50360461)x3	ABCD2, ADAMTS20 +92 more	Copy number gain	See cases	GPathogenic

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: 33