Related gene-specific medical variations for Gene (Select 9582) - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3127938	NM_004900.5(APOBEC3B):c.1121G>A (p.Arg374Gln)	APOBEC3B, APOBEC3B-AS1 (R374Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3127937	NM_004900.5(APOBEC3B):c.1051C>T (p.Arg351Cys)	APOBEC3B-AS1, APOBEC3B (R326C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540306	NM_004900.5(APOBEC3B):c.1069C>G (p.Gln357Glu)	APOBEC3B, APOBEC3B-AS1 (Q357E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381796	NM_004900.5(APOBEC3B):c.979C>T (p.Arg327Trp)	APOBEC3B, APOBEC3B-AS1 (R302W +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2312926	NM_004900.5(APOBEC3B):c.1072C>A (p.Pro358Thr)	APOBEC3B, APOBEC3B-AS1 (P333T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1050592	NM_004900.5(APOBEC3B):c.262A>C (p.Ile88Leu)	APOBEC3B, LOC126863151 (I88L)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 1050108	NM_004900.5(APOBEC3B):c.1052G>A (p.Arg351His)	APOBEC3B-AS1, APOBEC3B (R326H +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1049449	NM_004900.5(APOBEC3B):c.1026G>C (p.Glu342Asp)	APOBEC3B, APOBEC3B-AS1 (E317D +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign