Related gene-specific medical variations for Gene (Select 90589) - ClinVar - NCBI

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

Links from Gene

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258966	NM_145233.4(ZNF625):c.947C>T (p.Ser316Leu)	ZNF625, ZNF625-ZNF20 (S316L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197314	NM_145233.4(ZNF625):c.995A>G (p.Glu332Gly)	ZNF625, ZNF625-ZNF20 (E332G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197312	NM_145233.4(ZNF625):c.145G>A (p.Asp49Asn)	ZNF625, ZNF625-ZNF20 (D49N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2553070	NM_145233.4(ZNF625):c.770A>G (p.His257Arg)	ZNF625, ZNF625-ZNF20 (H257R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543127	NM_145233.4(ZNF625):c.860T>C (p.Phe287Ser)	ZNF625, ZNF625-ZNF20 (F287S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542573	NM_145233.4(ZNF625):c.230A>T (p.Asp77Val)	ZNF625, ZNF625-ZNF20 (D77V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541242	NM_145233.4(ZNF625):c.1072C>A (p.Pro358Thr)	ZNF625, ZNF625-ZNF20 (P358T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489415	NM_145233.4(ZNF625):c.910G>A (p.Glu304Lys)	ZNF625, ZNF625-ZNF20 (E304K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334192	NM_145233.4(ZNF625):c.1105G>C (p.Glu369Gln)	ZNF625, ZNF625-ZNF20 (E369Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334074	NM_145233.4(ZNF625):c.442C>T (p.Pro148Ser)	ZNF625, ZNF625-ZNF20 (P148S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2268986	NM_145233.4(ZNF625):c.956G>A (p.Arg319Gln)	ZNF625, ZNF625-ZNF20 (R319Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263547	NM_145233.4(ZNF625):c.317G>A (p.Ser106Asn)	ZNF625, ZNF625-ZNF20 (S106N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2259858	NM_145233.4(ZNF625):c.293G>A (p.Arg98Gln)	ZNF625, ZNF625-ZNF20 (R98Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256626	NM_145233.4(ZNF625):c.557G>C (p.Ser186Thr)	ZNF625, ZNF625-ZNF20 (S186T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance