Related gene-specific medical variations for Gene (Select 163131) - ClinVar

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Links from Gene

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259538	NM_001005851.3(ZNF780B):c.925G>A (p.Glu309Lys)	LOC126862908, ZNF780B (E309K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259537	NM_001005851.3(ZNF780B):c.788A>C (p.Asn263Thr)	LOC126862908, ZNF780B (N263T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259535	NM_001005851.3(ZNF780B):c.1001A>G (p.Glu334Gly)	LOC126862908, ZNF780B (E334G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198334	NM_001005851.3(ZNF780B):c.793A>G (p.Thr265Ala)	LOC126862908, ZNF780B (T265A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198333	NM_001005851.3(ZNF780B):c.725T>C (p.Ile242Thr)	LOC126862908, ZNF780B (I242T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198332	NM_001005851.3(ZNF780B):c.723C>A (p.Asn241Lys)	LOC126862908, ZNF780B (N241K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198331	NM_001005851.3(ZNF780B):c.266C>G (p.Ser89Cys)	LOC126862908, ZNF780B (S89C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198326	NM_001005851.3(ZNF780B):c.1306C>A (p.Gln436Lys)	LOC126862908, ZNF780B (Q436K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198324	NM_001005851.3(ZNF780B):c.1028C>T (p.Thr343Ile)	LOC126862908, ZNF780B (T343I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198323	NM_001005851.3(ZNF780B):c.1027A>G (p.Thr343Ala)	LOC126862908, ZNF780B (T343A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588111	NM_001005851.3(ZNF780B):c.305A>T (p.His102Leu)	LOC126862908, ZNF780B (H102L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560061	NM_001005851.3(ZNF780B):c.956A>C (p.Gln319Pro)	LOC126862908, ZNF780B (Q319P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536017	NM_001005851.3(ZNF780B):c.692A>G (p.Asn231Ser)	LOC126862908, ZNF780B (N231S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2533313	NM_001005851.3(ZNF780B):c.1001A>C (p.Glu334Ala)	LOC126862908, ZNF780B (E334A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455018	NM_001005851.3(ZNF780B):c.1022C>A (p.Ala341Asp)	LOC126862908, ZNF780B (A341D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378726	NM_001005851.3(ZNF780B):c.872A>G (p.Asn291Ser)	LOC126862908, ZNF780B (N291S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331140	NM_001005851.3(ZNF780B):c.538C>G (p.Leu180Val)	LOC126862908, ZNF780B (L180V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286275	NM_001005851.3(ZNF780B):c.883C>T (p.His295Tyr)	LOC126862908, ZNF780B (H295Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273737	NM_001005851.3(ZNF780B):c.1190C>G (p.Ser397Cys)	LOC126862908, ZNF780B (S397C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253198	NM_001005851.3(ZNF780B):c.1162C>T (p.Pro388Ser)	LOC126862908, ZNF780B (P388S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240016	NM_001005851.3(ZNF780B):c.1176A>T (p.Lys392Asn)	LOC126862908, ZNF780B (K392N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218434	NM_001005851.3(ZNF780B):c.347T>C (p.Phe116Ser)	LOC126862908, ZNF780B (F116S)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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Links from Gene

Items: 22