Related gene-specific medical variations for Gene (Select 51545) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258776	NM_207115.2(ZNF580):c.436G>A (p.Ala146Thr)	LOC125384545, ZNF580 +1 more (A146T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196913	NM_207115.2(ZNF580):c.199G>A (p.Val67Met)	LOC125384545, ZNF580 +1 more (V67M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609333	NM_207115.2(ZNF580):c.91A>C (p.Lys31Gln)	LOC125384545, ZNF580 +1 more (K31Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599070	NM_207115.2(ZNF580):c.473G>A (p.Arg158His)	LOC125384545, ZNF580 +1 more (R158H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538197	NM_207115.2(ZNF580):c.140C>T (p.Pro47Leu)	LOC125384545, ZNF580 +1 more (P47L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530457	NM_207115.2(ZNF580):c.455G>A (p.Cys152Tyr)	LOC125384545, ZNF580 +1 more (C152Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285186	NM_207115.2(ZNF580):c.380A>G (p.Lys127Arg)	LOC125384545, ZNF580 +1 more (K127R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233739	NM_207115.2(ZNF580):c.184C>T (p.Pro62Ser)	LOC125384545, ZNF580 +1 more (P62S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224620	NM_207115.2(ZNF580):c.76G>C (p.Ala26Pro)	LOC125384545, ZNF580 +1 more (A26P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 777510	NM_207115.2(ZNF580):c.244C>A (p.Pro82Thr)	LOC125384545, ZNF580 +1 more (P82T)	Single nucleotide variant (missense variant)	not provided	GBenign