Related gene-specific medical variations for Gene (Select 7753) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3194316	NM_003455.4(ZNF202):c.628G>A (p.Glu210Lys)	LOC126861372, ZNF202 (E210K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194315	NM_003455.4(ZNF202):c.572G>A (p.Arg191His)	LOC126861372, ZNF202 (R191H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194314	NM_003455.4(ZNF202):c.514G>A (p.Glu172Lys)	LOC126861372, ZNF202 (E172K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194313	NM_003455.4(ZNF202):c.506C>T (p.Ser169Leu)	LOC126861372, ZNF202 (S169L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2539155	NM_003455.4(ZNF202):c.491A>T (p.Asp164Val)	LOC126861372, ZNF202 (D164V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403315	NM_003455.4(ZNF202):c.666C>A (p.Asp222Glu)	LOC126861372, ZNF202 (D222E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380715	NM_003455.4(ZNF202):c.560C>T (p.Pro187Leu)	LOC126861372, ZNF202 (P187L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316025	NM_003455.4(ZNF202):c.466C>T (p.Pro156Ser)	LOC126861372, ZNF202 (P156S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 769811	NM_003455.4(ZNF202):c.462G>A (p.Val154=)	LOC126861372, ZNF202	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign