GOPC[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3100987	NM_020399.4(GOPC):c.907A>G (p.Ile303Val)	GOPC (I295V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602263	NM_020399.4(GOPC):c.761G>A (p.Arg254Gln)	GOPC (R254Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281980	NM_020399.4(GOPC):c.677G>A (p.Arg226Gln)	GOPC (R226Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100985	NM_020399.4(GOPC):c.482A>G (p.Glu161Gly)	GOPC (E153G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656876	NM_020399.4(GOPC):c.441G>A (p.Lys147=)	GOPC	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2460065	NM_020399.4(GOPC):c.374A>G (p.Gln125Arg)	GOPC (Q125R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325163	NM_020399.4(GOPC):c.215G>T (p.Ser72Ile)	GOPC (S72I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487244	NM_020399.4(GOPC):c.182A>G (p.Asp61Gly)	GOPC (D61G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527795	NM_020399.4(GOPC):c.162G>C (p.Glu54Asp)	GOPC (E54D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2656877	NM_020399.4(GOPC):c.158G>A (p.Gly53Glu)	GOPC (G53E)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2617223	NM_020399.4(GOPC):c.115A>G (p.Lys39Glu)	GOPC (K39E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334292	NM_020399.4(GOPC):c.68G>A (p.Gly23Glu)	GOPC (G23E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621171	NM_020399.4(GOPC):c.55T>C (p.Ser19Pro)	GOPC (S19P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100984	NM_020399.4(GOPC):c.46G>C (p.Gly16Arg)	GOPC (G16R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100986	NM_020399.4(GOPC):c.8C>T (p.Ala3Val)	GOPC (A3V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225515	NM_020399.4(GOPC):c.7G>A (p.Ala3Thr)	GOPC (A3T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance