GOLGA8A[gene] and "single gene"[properties] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2495021	NM_181077.5(GOLGA8A):c.1778T>C (p.Phe593Ser)	GOLGA8A (F592S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460868	NM_181077.5(GOLGA8A):c.1775G>T (p.Cys592Phe)	GOLGA8A (C591F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2262441	NM_181077.5(GOLGA8A):c.1765T>C (p.Cys589Arg)	GOLGA8A (C589R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3281921	NM_181077.5(GOLGA8A):c.1751T>C (p.Leu584Ser)	GOLGA8A (L584S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233755	NM_181077.5(GOLGA8A):c.1710G>C (p.Gln570His)	GOLGA8A (Q569H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 768693	NM_181077.5(GOLGA8A):c.1702G>A (p.Val568Ile)	GOLGA8A (V568I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2407718	NM_181077.5(GOLGA8A):c.1699C>G (p.Pro567Ala)	GOLGA8A (P566A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345424	NM_181077.5(GOLGA8A):c.1688C>G (p.Pro563Arg)	GOLGA8A (P562R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378661	NM_181077.5(GOLGA8A):c.1687C>T (p.Pro563Ser)	GOLGA8A (P562S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2645150	NM_181077.5(GOLGA8A):c.1623G>T (p.Ala541=)	GOLGA8A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3281923	NM_181077.5(GOLGA8A):c.1622C>T (p.Ala541Val)	GOLGA8A (A540V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2508574	NM_181077.5(GOLGA8A):c.1601A>G (p.Lys534Arg)	GOLGA8A (K534R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533092	NM_181077.5(GOLGA8A):c.1558A>G (p.Ser520Gly)	GOLGA8A (S519G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3281924	NM_181077.5(GOLGA8A):c.1537C>G (p.Arg513Gly)	GOLGA8A (R513G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3281922	NM_181077.5(GOLGA8A):c.1529C>T (p.Ala510Val)	GOLGA8A (A509V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359267	NM_181077.5(GOLGA8A):c.1507G>A (p.Glu503Lys)	GOLGA8A (E502K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2280053	NM_181077.5(GOLGA8A):c.1487C>T (p.Ala496Val)	GOLGA8A (A495V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391094	NM_181077.5(GOLGA8A):c.1402T>G (p.Ser468Ala)	GOLGA8A (S467A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2402501	NM_181077.5(GOLGA8A):c.297G>T (p.Lys99Asn)	GOLGA8A (K99N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211586	NM_181077.5(GOLGA8A):c.209C>T (p.Pro70Leu)	GOLGA8A (P70L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409401	NM_181077.5(GOLGA8A):c.199C>T (p.Arg67Cys)	GOLGA8A (R67C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596464	NM_181077.5(GOLGA8A):c.193C>T (p.His65Tyr)	GOLGA8A (H65Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362221	NM_181077.5(GOLGA8A):c.173C>T (p.Ser58Phe)	GOLGA8A (S58F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 23