Related gene-specific medical variations for Gene (Select 6478) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3318440	NM_005067.7(SIAH2):c.188G>T (p.Gly63Val)	SIAH2, SIAH2-AS1 (G63V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162052	NM_005067.7(SIAH2):c.31G>T (p.Ala11Ser)	SIAH2, SIAH2-AS1 (A11S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162051	NM_005067.7(SIAH2):c.229C>T (p.Leu77Phe)	SIAH2, SIAH2-AS1 (L77F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534559	NM_005067.7(SIAH2):c.47G>A (p.Ser16Asn)	SIAH2, SIAH2-AS1 (S16N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485625	NM_005067.7(SIAH2):c.41C>A (p.Pro14His)	SIAH2, SIAH2-AS1 (P14H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343497	NM_005067.7(SIAH2):c.80C>G (p.Pro27Arg)	SIAH2, SIAH2-AS1 (P27R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341509	NM_005067.7(SIAH2):c.224C>T (p.Thr75Ile)	SIAH2, SIAH2-AS1 (T75I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278748	NM_005067.7(SIAH2):c.94C>T (p.Pro32Ser)	SIAH2, SIAH2-AS1 (P32S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235034	NM_005067.7(SIAH2):c.35A>G (p.Asn12Ser)	SIAH2, SIAH2-AS1 (N12S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216592	NM_005067.7(SIAH2):c.19A>C (p.Thr7Pro)	SIAH2, SIAH2-AS1 (T7P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215027	NM_005067.7(SIAH2):c.130G>A (p.Gly44Ser)	SIAH2, SIAH2-AS1 (G44S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance