Related gene-specific medical variations for Gene (Select 729747) - ClinVar

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Links from Gene

Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259848	NM_001080404.3(ZNF878):c.304T>C (p.Tyr102His)	ZNF433-AS1, ZNF878 (Y102H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3259847	NM_001080404.3(ZNF878):c.677C>A (p.Pro226His)	ZNF433-AS1, ZNF878 (P226H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259846	NM_001080404.3(ZNF878):c.1097C>A (p.Pro366His)	ZNF433-AS1, ZNF878 (P366H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259845	NM_001080404.3(ZNF878):c.1585C>T (p.His529Tyr)	ZNF433-AS1, ZNF878 (H529Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259844	NM_001080404.3(ZNF878):c.527G>A (p.Cys176Tyr)	ZNF433-AS1, ZNF878 (C176Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259843	NM_001080404.3(ZNF878):c.1268A>G (p.Tyr423Cys)	ZNF433-AS1, ZNF878 (Y423C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259841	NM_001080404.3(ZNF878):c.784A>G (p.Lys262Glu)	ZNF433-AS1, ZNF878 (K262E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198941	NM_001080404.3(ZNF878):c.968C>G (p.Ser323Cys)	ZNF433-AS1, ZNF878 (S323C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198940	NM_001080404.3(ZNF878):c.962T>A (p.Ile321Asn)	ZNF433-AS1, ZNF878 (I321N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198939	NM_001080404.3(ZNF878):c.738G>T (p.Glu246Asp)	ZNF433-AS1, ZNF878 (E246D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198938	NM_001080404.3(ZNF878):c.590A>C (p.Lys197Thr)	ZNF433-AS1, ZNF878 (K197T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198937	NM_001080404.3(ZNF878):c.493C>T (p.His165Tyr)	ZNF433-AS1, ZNF878 (H165Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198935	NM_001080404.3(ZNF878):c.389T>G (p.Leu130Arg)	ZNF433-AS1, ZNF878 (L130R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198934	NM_001080404.3(ZNF878):c.1561A>G (p.Ile521Val)	ZNF433-AS1, ZNF878 (I521V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619618	NM_001080404.3(ZNF878):c.692T>A (p.Ile231Lys)	ZNF433-AS1, ZNF878 (I231K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604274	NM_001080404.3(ZNF878):c.475C>T (p.Arg159Cys)	ZNF433-AS1, ZNF878 (R159C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592027	NM_001080404.3(ZNF878):c.961A>G (p.Ile321Val)	ZNF433-AS1, ZNF878 (I321V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588993	NM_001080404.3(ZNF878):c.476G>A (p.Arg159His)	ZNF433-AS1, ZNF878 (R159H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569052	NM_001080404.3(ZNF878):c.200T>C (p.Ile67Thr)	ZNF433-AS1, ZNF878 (I67T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525758	NM_001080404.3(ZNF878):c.334A>G (p.Ile112Val)	ZNF433-AS1, ZNF878 (I112V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522743	NM_001080404.3(ZNF878):c.413C>G (p.Thr138Ser)	ZNF433-AS1, ZNF878 (T138S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494599	NM_001080404.3(ZNF878):c.736G>A (p.Glu246Lys)	ZNF433-AS1, ZNF878 (E246K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382588	NM_001080404.3(ZNF878):c.761G>A (p.Arg254His)	ZNF433-AS1, ZNF878 (R254H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355842	NM_001080404.3(ZNF878):c.793A>C (p.Asn265His)	ZNF433-AS1, ZNF878 (N265H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352327	NM_001080404.3(ZNF878):c.979C>T (p.Arg327Cys)	ZNF433-AS1, ZNF878 (R327C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308199	NM_001080404.3(ZNF878):c.1396A>G (p.Ile466Val)	ZNF433-AS1, ZNF878 (I466V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306436	NM_001080404.3(ZNF878):c.1426G>C (p.Glu476Gln)	ZNF433-AS1, ZNF878 (E476Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242704	NM_001080404.3(ZNF878):c.1247C>A (p.Thr416Asn)	ZNF433-AS1, ZNF878 (T416N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 28