Related gene-specific medical variations for Gene (Select 123207) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3312656	NM_031452.4(RAMAC):c.166A>C (p.Asn56His)	C15orf40, RAMAC (N56H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312655	NM_031452.4(RAMAC):c.220C>T (p.Pro74Ser)	C15orf40, RAMAC (P74S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312653	NM_031452.4(RAMAC):c.211T>G (p.Trp71Gly)	C15orf40, RAMAC (W71G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151350	NM_031452.4(RAMAC):c.72G>T (p.Lys24Asn)	C15orf40, RAMAC (K24N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151349	NM_031452.4(RAMAC):c.346G>A (p.Gly116Ser)	C15orf40, RAMAC (G116S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151348	NM_031452.4(RAMAC):c.319T>C (p.Tyr107His)	C15orf40, RAMAC (Y107H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151347	NM_031452.4(RAMAC):c.267C>A (p.Asn89Lys)	C15orf40, RAMAC (N89K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151346	NM_031452.4(RAMAC):c.246G>T (p.Trp82Cys)	C15orf40, RAMAC (W82C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151345	NM_031452.4(RAMAC):c.167A>G (p.Asn56Ser)	C15orf40, RAMAC (N56S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614719	NM_031452.4(RAMAC):c.178G>A (p.Asp60Asn)	C15orf40, RAMAC (D60N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480768	NM_031452.4(RAMAC):c.233G>A (p.Arg78Gln)	C15orf40, RAMAC (R78Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance