Related gene-specific medical variations for Gene (Select 7705) - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3334990	NM_007145.3(ZNF146):c.343C>T (p.Leu115Phe)	ZNF146, ZNF565 (L115F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194091	NM_007145.3(ZNF146):c.778A>G (p.Arg260Gly)	ZNF146, ZNF565 (R260G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194090	NM_007145.3(ZNF146):c.471A>T (p.Lys157Asn)	ZNF146, ZNF565 (K157N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

Format

Sort by

Choose Destination

ClinVar