Related gene-specific medical variations for Gene (Select 25850) - ClinVar

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Links from Gene

Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3198662	NM_001037232.4(ZNF829):c.754T>C (p.Cys252Arg)	LOC126862899, ZNF345 +1 more (C333R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198658	NM_001037232.4(ZNF829):c.1161G>T (p.Lys387Asn)	LOC126862899, ZNF345 +1 more (K387N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195313	NM_001242472.2(ZNF345):c.826C>T (p.His276Tyr)	LOC126862898, ZNF345 (H276Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195311	NM_001242472.2(ZNF345):c.758C>G (p.Thr253Ser)	LOC126862898, ZNF345 (T253S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195310	NM_001242472.2(ZNF345):c.700G>C (p.Ala234Pro)	LOC126862898, ZNF345 (A234P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195309	NM_001242472.2(ZNF345):c.664C>T (p.Arg222Trp)	LOC126862898, ZNF345 (R222W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195308	NM_001242472.2(ZNF345):c.635G>A (p.Gly212Asp)	LOC126862898, ZNF345 (G212D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195302	NM_001242472.2(ZNF345):c.1367G>A (p.Cys456Tyr)	LOC126862898, ZNF345 (C456Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195301	NM_001242472.2(ZNF345):c.1115G>A (p.Cys372Tyr)	LOC126862898, ZNF345 (C372Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2649766	NM_001037232.4(ZNF829):c.1140T>C (p.Tyr380=)	LOC126862899, ZNF345 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2600492	NM_001242472.2(ZNF345):c.941A>T (p.Tyr314Phe)	LOC126862898, ZNF345 (Y314F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595998	NM_001037232.4(ZNF829):c.670A>G (p.Ser224Gly)	LOC126862899, ZNF345 +1 more (S224G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542709	NM_001037232.4(ZNF829):c.1258C>T (p.Arg420Cys)	LOC126862899, ZNF345 +1 more (R420C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542338	NM_001242472.2(ZNF345):c.1418A>G (p.Lys473Arg)	LOC126862898, ZNF345 (K473R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517193	NM_001242472.2(ZNF345):c.1459A>G (p.Ile487Val)	LOC126862898, ZNF345 (I487V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490636	NM_001242472.2(ZNF345):c.1181G>A (p.Gly394Asp)	LOC126862898, ZNF345 (G394D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477657	NM_001242472.2(ZNF345):c.1235C>G (p.Ala412Gly)	LOC126862898, ZNF345 (A412G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463697	NM_001037232.4(ZNF829):c.1025A>G (p.His342Arg)	LOC126862899, ZNF345 +1 more (H423R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458374	NM_001242472.2(ZNF345):c.1204G>C (p.Glu402Gln)	LOC126862898, ZNF345 (E402Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411645	NM_001037232.4(ZNF829):c.993G>C (p.Lys331Asn)	LOC126862899, ZNF345 +1 more (K412N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403751	NM_001242472.2(ZNF345):c.838C>A (p.His280Asn)	LOC126862898, ZNF345 (H280N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401550	NM_001242472.2(ZNF345):c.662G>A (p.Arg221Gln)	LOC126862898, ZNF345 (R221Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385613	NM_001037232.4(ZNF829):c.839G>A (p.Ser280Asn)	LOC126862899, ZNF345 +1 more (S280N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382240	NM_001037232.4(ZNF829):c.584G>A (p.Arg195His)	LOC126862899, ZNF345 +1 more (R195H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364796	NM_001242472.2(ZNF345):c.1061G>A (p.Gly354Asp)	LOC126862898, ZNF345 (G354D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312725	NM_001242472.2(ZNF345):c.1409A>G (p.Gln470Arg)	LOC126862898, ZNF345 (Q470R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306775	NM_001037232.4(ZNF829):c.1054T>A (p.Tyr352Asn)	LOC126862899, ZNF345 +1 more (Y352N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291616	NM_001037232.4(ZNF829):c.586G>C (p.Gly196Arg)	LOC126862899, ZNF345 +1 more (G196R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240909	NM_001037232.4(ZNF829):c.483T>G (p.Cys161Trp)	LOC126862899, ZNF345 +1 more (C161W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233149	NM_001037232.4(ZNF829):c.391C>T (p.Arg131Cys)	LOC126862899, ZNF345 +1 more (R212C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215587	NM_001242472.2(ZNF345):c.1147T>C (p.Ser383Pro)	LOC126862898, ZNF345 (S383P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213237	NM_001242472.2(ZNF345):c.685C>T (p.Pro229Ser)	LOC126862898, ZNF345 (P229S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 789119	NM_001242472.2(ZNF345):c.803G>C (p.Ser268Thr)	LOC126862898, ZNF345 (S268T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 787487	NM_001242472.2(ZNF345):c.1450T>C (p.Leu484=)	LOC126862898, ZNF345	Single nucleotide variant (synonymous variant)	not provided	GBenign

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Links from Gene

Items: 34