"Ambry Genetics"[submitter] AND "ZNF467"[gene] - ClinVar

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

Search results

Items: 66

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3195958	NM_207336.3(ZNF467):c.1780T>C (p.Phe594Leu)	ZNF467 (F594L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195957	NM_207336.3(ZNF467):c.1772C>T (p.Pro591Leu)	ZNF467 (P591L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346718	NM_207336.3(ZNF467):c.1757C>G (p.Pro586Arg)	ZNF467 (P586R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214168	NM_207336.3(ZNF467):c.1756C>T (p.Pro586Ser)	ZNF467 (P586S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213929	NM_207336.3(ZNF467):c.1696G>A (p.Gly566Ser)	ZNF467 (G566S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2600130	NM_207336.3(ZNF467):c.1678C>T (p.Arg560Trp)	ZNF467 (R560W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490832	NM_207336.3(ZNF467):c.1646G>A (p.Gly549Glu)	ZNF467 (G549E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353549	NM_207336.3(ZNF467):c.1577C>G (p.Ser526Cys)	ZNF467 (S526C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314622	NM_207336.3(ZNF467):c.1573A>T (p.Ser525Cys)	ZNF467 (S525C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401159	NM_207336.3(ZNF467):c.1504C>G (p.Leu502Val)	ZNF467 (L502V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195956	NM_207336.3(ZNF467):c.1503C>G (p.His501Gln)	ZNF467 (H501Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513394	NM_207336.3(ZNF467):c.1501C>G (p.His501Asp)	ZNF467 (H501D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226400	NM_207336.3(ZNF467):c.1492C>A (p.Arg498Ser)	ZNF467 (R498S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357220	NM_207336.3(ZNF467):c.1455G>C (p.Arg485Ser)	ZNF467 (R485S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195954	NM_207336.3(ZNF467):c.1447G>A (p.Gly483Ser)	ZNF467 (G483S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534792	NM_207336.3(ZNF467):c.1394A>G (p.Asp465Gly)	ZNF467 (D465G)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2534790	NM_207336.3(ZNF467):c.1384A>G (p.Thr462Ala)	ZNF467 (T462A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2618604	NM_207336.3(ZNF467):c.1373C>T (p.Pro458Leu)	ZNF467 (P458L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557166	NM_207336.3(ZNF467):c.1292T>C (p.Phe431Ser)	ZNF467 (F431S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258185	NM_207336.3(ZNF467):c.1259T>C (p.Val420Ala)	ZNF467 (V420A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3195953	NM_207336.3(ZNF467):c.1237G>C (p.Gly413Arg)	ZNF467 (G413R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484082	NM_207336.3(ZNF467):c.1215C>A (p.Ser405Arg)	ZNF467 (S405R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195952	NM_207336.3(ZNF467):c.1214G>C (p.Ser405Thr)	ZNF467 (S405T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2268390	NM_207336.3(ZNF467):c.1174G>T (p.Gly392Cys)	ZNF467 (G392C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258183	NM_207336.3(ZNF467):c.1138G>A (p.Glu380Lys)	ZNF467 (E380K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195951	NM_207336.3(ZNF467):c.1100A>G (p.Lys367Arg)	ZNF467 (K367R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613678	NM_207336.3(ZNF467):c.1022C>T (p.Thr341Ile)	ZNF467 (T341I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258184	NM_207336.3(ZNF467):c.768G>C (p.Lys256Asn)	ZNF467 (K256N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548580	NM_207336.3(ZNF467):c.725G>T (p.Arg242Leu)	ZNF467 (R242L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195963	NM_207336.3(ZNF467):c.721G>A (p.Glu241Lys)	ZNF467 (E241K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533842	NM_207336.3(ZNF467):c.719G>A (p.Gly240Asp)	ZNF467 (G240D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258180	NM_207336.3(ZNF467):c.681G>C (p.Lys227Asn)	ZNF467 (K227N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490114	NM_207336.3(ZNF467):c.661T>C (p.Cys221Arg)	ZNF467 (C221R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457216	NM_207336.3(ZNF467):c.650C>T (p.Pro217Leu)	ZNF467 (P217L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2539028	NM_207336.3(ZNF467):c.632G>A (p.Arg211His)	ZNF467 (R211H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258181	NM_207336.3(ZNF467):c.627C>G (p.Ser209Arg)	ZNF467 (S209R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208853	NM_207336.3(ZNF467):c.583C>T (p.Arg195Cys)	ZNF467 (R195C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220881	NM_207336.3(ZNF467):c.581G>A (p.Gly194Asp)	ZNF467 (G194D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195962	NM_207336.3(ZNF467):c.574G>C (p.Asp192His)	ZNF467 (D192H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195961	NM_207336.3(ZNF467):c.571C>A (p.Pro191Thr)	ZNF467 (P191T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258182	NM_207336.3(ZNF467):c.559C>G (p.Pro187Ala)	ZNF467 (P187A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459572	NM_207336.3(ZNF467):c.551G>C (p.Gly184Ala)	ZNF467 (G184A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367655	NM_207336.3(ZNF467):c.547C>T (p.Arg183Trp)	ZNF467 (R183W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195960	NM_207336.3(ZNF467):c.467C>G (p.Pro156Arg)	ZNF467 (P156R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267546	NM_207336.3(ZNF467):c.400T>A (p.Tyr134Asn)	ZNF467 (Y134N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195959	NM_207336.3(ZNF467):c.359G>T (p.Ser120Ile)	ZNF467 (S120I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463364	NM_207336.3(ZNF467):c.334C>A (p.Pro112Thr)	ZNF467 (P112T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485734	NM_207336.3(ZNF467):c.333G>T (p.Trp111Cys)	ZNF467 (W111C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390600	NM_207336.3(ZNF467):c.325G>T (p.Val109Phe)	ZNF467 (V109F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511144	NM_207336.3(ZNF467):c.298G>A (p.Asp100Asn)	ZNF467 (D100N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339529	NM_207336.3(ZNF467):c.265G>A (p.Glu89Lys)	ZNF467 (E89K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462839	NM_207336.3(ZNF467):c.208T>C (p.Cys70Arg)	ZNF467 (C70R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480692	NM_207336.3(ZNF467):c.178G>A (p.Gly60Ser)	ZNF467 (G60S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333861	NM_207336.3(ZNF467):c.178G>T (p.Gly60Cys)	ZNF467 (G60C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527383	NM_207336.3(ZNF467):c.170C>T (p.Pro57Leu)	ZNF467 (P57L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2247315	NM_207336.3(ZNF467):c.60G>C (p.Met20Ile)	ZNF467 (M20I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3170463	NR_163594.1(SSPO):n.53G>A	ZNF467	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2370929	NR_163594.1(SSPO):n.74C>G	ZNF467	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2457922	NR_163594.1(SSPO):n.76A>C	ZNF467	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2457923	NR_163594.1(SSPO):n.80G>A	ZNF467	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 3322844	NR_163594.1(SSPO):n.149G>T	ZNF467	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2293317	NR_163594.1(SSPO):n.160C>T	ZNF467	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2258773	NR_163594.1(SSPO):n.179G>A	ZNF467	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2470963	NR_163594.1(SSPO):n.185G>A	ZNF467	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 2341297	NR_163594.1(SSPO):n.185G>T	ZNF467	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2569246	NR_163594.1(SSPO):n.197C>T	ZNF467	Single nucleotide variant (non-coding transcript 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: 66