"Ambry Genetics"[submitter] AND "ZNF875"[gene] - ClinVar

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

Search results

Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2513195	NM_001353803.2(ZNF875):c.34-2441G>A	ZNF875 (S22N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198932	NM_001353803.2(ZNF875):c.34-2417C>T	ZNF875 (T30M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473968	NM_001353803.2(ZNF875):c.35C>T (p.Ala12Val)	ZNF875 (A12V +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3259836	NM_001353803.2(ZNF875):c.58G>A (p.Ala20Thr)	ZNF875 (A14T +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3198924	NM_001353803.2(ZNF875):c.178C>G (p.Pro60Ala)	ZNF875 (P18A +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3259839	NM_001353803.2(ZNF875):c.208G>A (p.Glu70Lys)	ZNF875 (E56K +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3259840	NM_001353803.2(ZNF875):c.224A>G (p.Glu75Gly)	ZNF875 (E61G +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3198925	NM_001353803.2(ZNF875):c.280A>T (p.Ser94Cys)	ZNF875 (S52C +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2522560	NM_001353803.2(ZNF875):c.350C>G (p.Ser117Cys)	ZNF875 (S118C +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198926	NM_001353803.2(ZNF875):c.359T>G (p.Phe120Cys)	ZNF875 (F107C +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198927	NM_001353803.2(ZNF875):c.383C>G (p.Pro128Arg)	ZNF875 (P114R +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198928	NM_001353803.2(ZNF875):c.431A>T (p.Asp144Val)	ZNF875 (D49V +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259835	NM_001353803.2(ZNF875):c.441C>G (p.Cys147Trp)	ZNF875 (C147W +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198929	NM_001353803.2(ZNF875):c.495T>G (p.Phe165Leu)	ZNF875 (F124L +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198930	NM_001353803.2(ZNF875):c.502G>A (p.Val168Ile)	ZNF875 (V126I +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198931	NM_001353803.2(ZNF875):c.529C>T (p.Leu177Phe)	ZNF875 (L171F +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2569086	NM_001353803.2(ZNF875):c.832G>A (p.Gly278Arg)	ZNF875 (G183R +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198933	NM_001353803.2(ZNF875):c.851G>T (p.Cys284Phe)	ZNF875 (C189F +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460260	NM_001353803.2(ZNF875):c.911A>G (p.His304Arg)	ZNF875 (H298R +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599859	NM_001353803.2(ZNF875):c.989G>A (p.Arg330Gln)	ZNF875 (R289Q +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623649	NM_001353803.2(ZNF875):c.1081A>G (p.Thr361Ala)	ZNF875 (T320A +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198912	NM_001353803.2(ZNF875):c.1117C>T (p.Arg373Cys)	ZNF875 (R278C +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198913	NM_001353803.2(ZNF875):c.1126C>T (p.Arg376Cys)	ZNF875 (R376C +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198914	NM_001353803.2(ZNF875):c.1127G>A (p.Arg376His)	ZNF875 (R362H +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488198	NM_001353803.2(ZNF875):c.1157G>A (p.Arg386Lys)	ZNF875 (R367K +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518730	NM_001353803.2(ZNF875):c.1171G>A (p.Glu391Lys)	ZNF875 (E385K +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198915	NM_001353803.2(ZNF875):c.1183A>G (p.Ile395Val)	ZNF875 (I376V +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3259838	NM_001353803.2(ZNF875):c.1265A>G (p.Tyr422Cys)	ZNF875 (Y380C +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198916	NM_001353803.2(ZNF875):c.1429C>G (p.Pro477Ala)	ZNF875 (P477A +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198917	NM_001353803.2(ZNF875):c.1454G>A (p.Arg485Gln)	ZNF875 (R443Q +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198918	NM_001353803.2(ZNF875):c.1457G>A (p.Gly486Asp)	ZNF875 (G391D +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471723	NM_001353803.2(ZNF875):c.1549G>T (p.Asp517Tyr)	ZNF875 (D476Y +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198919	NM_001353803.2(ZNF875):c.1630C>T (p.Arg544Trp)	ZNF875 (R502W +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198920	NM_001353803.2(ZNF875):c.1692G>C (p.Glu564Asp)	ZNF875 (E522D +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259837	NM_001353803.2(ZNF875):c.1723C>G (p.Leu575Val)	ZNF875 (L556V +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198921	NM_001353803.2(ZNF875):c.1735C>G (p.Gln579Glu)	ZNF875 (Q537E +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198922	NM_001353803.2(ZNF875):c.1747G>A (p.Ala583Thr)	ZNF875 (A542T +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541009	NM_001353803.2(ZNF875):c.1753G>A (p.Gly585Arg)	ZNF875 (G490R +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615093	NM_001353803.2(ZNF875):c.1844C>A (p.Pro615His)	ZNF875 (P610H +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198923	NM_001353803.2(ZNF875):c.1856G>T (p.Arg619Ile)	ZNF875 (R577I +10 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469450	NM_001353803.2(ZNF875):c.1868G>A (p.Arg623Gln)	ZNF875 (R604Q +10 more)	Single nucleotide variant (missense variant +1 more)	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: 41