C8orf74[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2335477	NM_001040032.2(C8orf74):c.68G>A (p.Arg23His)	C8orf74 (R23H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2368916	NM_001040032.2(C8orf74):c.362A>C (p.His121Pro)	C8orf74 (H121P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344684	NM_001040032.2(C8orf74):c.645A>C (p.Arg215Ser)	C8orf74 (R215S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372831	NM_001040032.2(C8orf74):c.647A>C (p.Gln216Pro)	C8orf74 (Q216P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220371	NM_001040032.2(C8orf74):c.787A>C (p.Thr263Pro)	C8orf74 (T263P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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