"Ambry Genetics"[submitter] AND "ZNF418"[gene] - ClinVar

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

Search results

Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2212961	NM_133460.3(ZNF418):c.1999A>G (p.Arg667Gly)	ZNF418 (R688G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593234	NM_133460.3(ZNF418):c.1993C>T (p.His665Tyr)	ZNF418 (H666Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406445	NM_133460.3(ZNF418):c.1976G>C (p.Ser659Thr)	ZNF418 (S659T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406444	NM_133460.3(ZNF418):c.1973G>A (p.Arg658Gln)	ZNF418 (R573Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550255	NM_133460.3(ZNF418):c.1946G>T (p.Cys649Phe)	ZNF418 (C650F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328075	NM_133460.3(ZNF418):c.1870T>C (p.Cys624Arg)	ZNF418 (C625R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195636	NM_133460.3(ZNF418):c.1583A>G (p.His528Arg)	ZNF418 (H528R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195635	NM_133460.3(ZNF418):c.1580G>A (p.Arg527Gln)	ZNF418 (R528Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511184	NM_133460.3(ZNF418):c.1495G>A (p.Val499Ile)	ZNF418 (V520I +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2462955	NM_133460.3(ZNF418):c.1459T>C (p.Cys487Arg)	ZNF418 (C402R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195634	NM_133460.3(ZNF418):c.1411G>A (p.Glu471Lys)	ZNF418 (E472K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195633	NM_133460.3(ZNF418):c.1337G>A (p.Arg446Gln)	ZNF418 (R361Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360279	NM_133460.3(ZNF418):c.1318A>G (p.Asn440Asp)	ZNF418 (N355D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392394	NM_133460.3(ZNF418):c.1279G>A (p.Glu427Lys)	ZNF418 (E342K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195631	NM_133460.3(ZNF418):c.1226G>A (p.Arg409Gln)	ZNF418 (R324Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337405	NM_133460.3(ZNF418):c.1192T>C (p.Tyr398His)	ZNF418 (Y399H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195630	NM_133460.3(ZNF418):c.1185A>C (p.Glu395Asp)	ZNF418 (E396D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263545	NM_133460.3(ZNF418):c.1093A>G (p.Thr365Ala)	ZNF418 (T365A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195629	NM_133460.3(ZNF418):c.1027G>C (p.Glu343Gln)	ZNF418 (E258Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591469	NM_133460.3(ZNF418):c.917G>A (p.Arg306Gln)	ZNF418 (R306Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278914	NM_133460.3(ZNF418):c.868G>C (p.Glu290Gln)	ZNF418 (E205Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216395	NM_133460.3(ZNF418):c.853C>T (p.Pro285Ser)	ZNF418 (P285S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195639	NM_133460.3(ZNF418):c.833G>A (p.Arg278Gln)	ZNF418 (R299Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588939	NM_133460.3(ZNF418):c.773A>G (p.Tyr258Cys)	ZNF418 (Y258C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195638	NM_133460.3(ZNF418):c.728A>G (p.Asp243Gly)	ZNF418 (D158G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518617	NM_133460.3(ZNF418):c.650T>C (p.Val217Ala)	ZNF418 (V217A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211025	NM_133460.3(ZNF418):c.631C>T (p.His211Tyr)	ZNF418 (H232Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329201	NM_133460.3(ZNF418):c.605A>G (p.His202Arg)	ZNF418 (H117R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558796	NM_133460.3(ZNF418):c.604C>T (p.His202Tyr)	ZNF418 (H223Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236966	NM_133460.3(ZNF418):c.574T>C (p.Cys192Arg)	ZNF418 (C107R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541870	NM_133460.3(ZNF418):c.297T>A (p.Asp99Glu)	ZNF418 (D120E +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2535608	NM_133460.3(ZNF418):c.287A>C (p.His96Pro)	ZNF418 (H11P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476404	NM_133460.3(ZNF418):c.163G>T (p.Ala55Ser)	ZNF418 (A76S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372461	NM_133460.3(ZNF418):c.125C>A (p.Ser42Tyr)	ZNF418 (S42Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195632	NM_133460.3(ZNF418):c.122T>C (p.Ile41Thr)	ZNF418 (I41T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195640	NM_133460.3(ZNF418):c.83G>T (p.Cys28Phe)	ZNF418 (C49F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551728	NM_133460.3(ZNF418):c.58A>G (p.Ser20Gly)	ZNF418 (S21G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign

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: 37