ZNF257[gene] and "single gene"[properties] - ClinVar

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

Search results

Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146659	GRCh38/hg38 19p12(chr19:22071063-22118991)x1	ZNF257	Copy number loss	See cases	GBenign
Select item 2232658	NM_033468.4(ZNF257):c.18T>G (p.Ile6Met)	ZNF257 (I6M)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2232329	NM_033468.4(ZNF257):c.139G>C (p.Val47Leu)	ZNF257 (V15L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2328690	NM_033468.4(ZNF257):c.145A>G (p.Lys49Glu)	ZNF257 (K17E +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2618494	NM_033468.4(ZNF257):c.157A>G (p.Ile53Val)	ZNF257 (I53V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2454682	NM_033468.4(ZNF257):c.169G>C (p.Glu57Gln)	ZNF257 (E25Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2290123	NM_033468.4(ZNF257):c.290A>T (p.Lys97Ile)	ZNF257 (K21I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194717	NM_033468.4(ZNF257):c.291A>T (p.Lys97Asn)	ZNF257 (K65N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306265	NM_033468.4(ZNF257):c.347G>A (p.Gly116Asp)	ZNF257 (G40D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404780	NM_033468.4(ZNF257):c.364G>C (p.Glu122Gln)	ZNF257 (E90Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213001	NM_033468.4(ZNF257):c.440G>A (p.Cys147Tyr)	ZNF257 (C115Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368562	NM_033468.4(ZNF257):c.487C>T (p.His163Tyr)	ZNF257 (H163Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335274	NM_033468.4(ZNF257):c.494T>C (p.Ile165Thr)	ZNF257 (I133T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194718	NM_033468.4(ZNF257):c.619G>A (p.Gly207Ser)	ZNF257 (G175S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194719	NM_033468.4(ZNF257):c.739C>A (p.His247Asn)	ZNF257 (H247N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302552	NM_033468.4(ZNF257):c.836A>T (p.His279Leu)	ZNF257 (H279L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339857	NM_033468.4(ZNF257):c.886T>C (p.Trp296Arg)	ZNF257 (W220R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545244	NM_033468.4(ZNF257):c.968A>C (p.Lys323Thr)	ZNF257 (K247T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194714	NM_033468.4(ZNF257):c.1085A>G (p.His362Arg)	ZNF257 (H286R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548305	NM_033468.4(ZNF257):c.1249A>C (p.Thr417Pro)	ZNF257 (T385P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335271	NM_033468.4(ZNF257):c.1288C>A (p.Pro430Thr)	ZNF257 (P398T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330996	NM_033468.4(ZNF257):c.1355T>C (p.Ile452Thr)	ZNF257 (I376T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194715	NM_033468.4(ZNF257):c.1373C>T (p.Pro458Leu)	ZNF257 (P382L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459592	NM_033468.4(ZNF257):c.1384G>A (p.Glu462Lys)	ZNF257 (E386K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483117	NM_033468.4(ZNF257):c.1423A>T (p.Thr475Ser)	ZNF257 (T399S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457627	NM_033468.4(ZNF257):c.1444A>G (p.Thr482Ala)	ZNF257 (T450A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335272	NM_033468.4(ZNF257):c.1492C>G (p.Arg498Gly)	ZNF257 (R466G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345295	NM_033468.4(ZNF257):c.1492C>T (p.Arg498Trp)	ZNF257 (R422W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335273	NM_033468.4(ZNF257):c.1493G>T (p.Arg498Leu)	ZNF257 (R498L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370514	NM_033468.4(ZNF257):c.1558T>C (p.Cys520Arg)	ZNF257 (C444R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472148	NM_033468.4(ZNF257):c.1561G>T (p.Gly521Cys)	ZNF257 (G445C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227200	NM_033468.4(ZNF257):c.1609C>T (p.His537Tyr)	ZNF257 (H461Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335270	NM_033468.4(ZNF257):c.1628A>G (p.Asn543Ser)	ZNF257 (N467S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554936	NM_033468.4(ZNF257):c.1680A>T (p.Lys560Asn)	ZNF257 (K484N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608078	NM_033468.4(ZNF257):c.1687T>C (p.Ser563Pro)	ZNF257 (S563P +2 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: 35