"Ambry Genetics"[submitter] AND "ZNF429"[gene] - ClinVar

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

Search results

Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2303962	NM_001001415.4(ZNF429):c.122T>C (p.Val41Ala)	ZNF429 (V41A +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2303764	NM_001001415.4(ZNF429):c.185C>A (p.Pro62His)	ZNF429 (P60H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2491401	NM_001001415.4(ZNF429):c.316C>T (p.Arg106Cys)	ZNF429 (R106C +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2537128	NM_001001415.4(ZNF429):c.376T>C (p.Tyr126His)	ZNF429 (Y124H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2525947	NM_001001415.4(ZNF429):c.434A>G (p.Tyr145Cys)	ZNF429 (Y81C +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2611260	NM_001001415.4(ZNF429):c.478G>A (p.Ala160Thr)	ZNF429 (A128T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2369850	NM_001001415.4(ZNF429):c.493A>G (p.Thr165Ala)	ZNF429 (T101A +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2521397	NM_001001415.4(ZNF429):c.503C>T (p.Thr168Ile)	ZNF429 (T168I +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2326675	NM_001001415.4(ZNF429):c.650C>A (p.Thr217Asn)	ZNF429 (T153N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2327568	NM_001001415.4(ZNF429):c.662G>C (p.Arg221Thr)	ZNF429 (R189T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2213661	NM_001001415.4(ZNF429):c.971G>A (p.Arg324Gln)	ZNF429 (R324Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2292520	NM_001001415.4(ZNF429):c.1004A>C (p.His335Pro)	ZNF429 (H303P +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355259	NM_001001415.4(ZNF429):c.1106A>G (p.Tyr369Cys)	ZNF429 (Y305C +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2203957	NM_001001415.4(ZNF429):c.1160A>G (p.His387Arg)	ZNF429 (H323R +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2554135	NM_001001415.4(ZNF429):c.1303A>G (p.Thr435Ala)	ZNF429 (T435A +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2217116	NM_001001415.4(ZNF429):c.1340A>G (p.His447Arg)	ZNF429 (H447R +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2522212	NM_001001415.4(ZNF429):c.1391G>A (p.Arg464Gln)	ZNF429 (R462Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2266863	NM_001001415.4(ZNF429):c.1486C>T (p.Leu496Phe)	ZNF429 (L432F +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2364522	NM_001001415.4(ZNF429):c.1643G>A (p.Arg548Gln)	ZNF429 (R548Q +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2230496	NM_001001415.4(ZNF429):c.1726C>T (p.His576Tyr)	ZNF429 (H544Y +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2388958	NM_001001415.4(ZNF429):c.1800A>C (p.Lys600Asn)	ZNF429 (K600N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2554136	NM_001001415.4(ZNF429):c.1892C>A (p.Thr631Asn)	ZNF429 (T567N +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2222143	NM_001001415.4(ZNF429):c.1942G>C (p.Val648Leu)	ZNF429 (V584L +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2404709	NM_001001415.4(ZNF429):c.1960C>T (p.Pro654Ser)	ZNF429 (P590S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2405432	NM_001001415.4(ZNF429):c.1982G>A (p.Gly661Asp)	ZNF429 (G597D +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2395689	NM_001001415.4(ZNF429):c.1987C>T (p.Arg663Trp)	ZNF429 (R631W +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	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: 26