"Ambry Genetics"[submitter] AND "ZNF155"[gene] - ClinVar

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

Search results

Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2512733	NM_198089.3(ZNF155):c.5C>T (p.Thr2Ile)	ZNF155 (T2I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2259665	NM_198089.3(ZNF155):c.149A>G (p.Gln50Arg)	ZNF155 (Q61R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328073	NM_198089.3(ZNF155):c.227G>A (p.Gly76Glu)	ZNF155 (G76E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525223	NM_198089.3(ZNF155):c.274G>A (p.Ala92Thr)	ZNF155 (A92T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526955	NM_198089.3(ZNF155):c.395C>T (p.Ser132Phe)	ZNF155 (S132F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459406	NM_198089.3(ZNF155):c.401T>C (p.Val134Ala)	ZNF155 (V145A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194108	NM_198089.3(ZNF155):c.455A>G (p.Lys152Arg)	ZNF155 (K152R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194109	NM_198089.3(ZNF155):c.598G>A (p.Gly200Arg)	ZNF155 (G200R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334998	NM_198089.3(ZNF155):c.612T>G (p.Phe204Leu)	ZNF155 (F215L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334929	NM_198089.3(ZNF155):c.634G>A (p.Glu212Lys)	ZNF155 (E223K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519738	NM_198089.3(ZNF155):c.677A>G (p.His226Arg)	ZNF155 (H237R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194110	NM_198089.3(ZNF155):c.728G>A (p.Arg243His)	ZNF155 (R243H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466077	NM_198089.3(ZNF155):c.744T>A (p.Asn248Lys)	ZNF155 (N248K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194111	NM_198089.3(ZNF155):c.805T>C (p.Phe269Leu)	ZNF155 (F280L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252852	NM_198089.3(ZNF155):c.822G>T (p.Gln274His)	ZNF155 (Q285H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2537212	NM_198089.3(ZNF155):c.842T>A (p.Ile281Asn)	ZNF155 (I281N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194112	NM_198089.3(ZNF155):c.850G>T (p.Gly284Trp)	ZNF155 (G295W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525655	NM_198089.3(ZNF155):c.877T>C (p.Cys293Arg)	ZNF155 (C293R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389180	NM_198089.3(ZNF155):c.943C>T (p.Pro315Ser)	ZNF155 (P315S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194114	NM_198089.3(ZNF155):c.998G>T (p.Arg333Met)	ZNF155 (R344M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368893	NM_198089.3(ZNF155):c.1036T>A (p.Cys346Ser)	ZNF155 (C346S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194105	NM_198089.3(ZNF155):c.1042C>G (p.Gln348Glu)	ZNF155, ZNF230-DT (Q348E +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2524828	NM_198089.3(ZNF155):c.1105G>A (p.Glu369Lys)	ZNF155, ZNF230-DT (E369K +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2267321	NM_198089.3(ZNF155):c.1196G>A (p.Ser399Asn)	ZNF155, ZNF230-DT (S399N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2531387	NM_198089.3(ZNF155):c.1307G>A (p.Gly436Asp)	ZNF155, ZNF230-DT (G436D +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3194107	NM_198089.3(ZNF155):c.1310A>C (p.Tyr437Ser)	ZNF155, ZNF230-DT (Y437S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2385082	NM_198089.3(ZNF155):c.1312G>A (p.Val438Ile)	ZNF155, ZNF230-DT (V438I +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2385083	NM_198089.3(ZNF155):c.1316C>G (p.Thr439Ser)	ZNF155, ZNF230-DT (T450S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2408723	NM_198089.3(ZNF155):c.1333T>A (p.Leu445Met)	ZNF155, ZNF230-DT (L445M +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2511551	NM_198089.3(ZNF155):c.1381T>G (p.Cys461Gly)	ZNF155, ZNF230-DT (C461G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2489178	NM_198089.3(ZNF155):c.1406C>T (p.Ser469Leu)	ZNF230-DT, ZNF155 (S469L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2495711	NM_198089.3(ZNF155):c.1427G>A (p.Arg476Lys)	ZNF155, ZNF230-DT (R487K +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2378853	NM_198089.3(ZNF155):c.1457G>A (p.Cys486Tyr)	ZNF155, ZNF230-DT (C486Y +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2613183	NM_198089.3(ZNF155):c.1477C>T (p.Leu493Phe)	ZNF155, ZNF230-DT (L493F +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2550592	NM_198089.3(ZNF155):c.1480G>C (p.Val494Leu)	ZNF155, ZNF230-DT (V494L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2349876	NM_198089.3(ZNF155):c.1495C>G (p.Arg499Gly)	ZNF155, ZNF230-DT (R499G +1 more)	Single nucleotide variant (non-coding transcript 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: 36