ClinVar Miner

List of variants in gene APOBEC2 studied for not specified

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_006789.4(APOBEC2):c.363G>C (p.Trp121Cys) rs549324782 0.00011
NM_006789.4(APOBEC2):c.643T>A (p.Tyr215Asn) rs374264492 0.00005
NM_006789.4(APOBEC2):c.346C>T (p.Arg116Trp) rs773387831 0.00002
NM_006789.4(APOBEC2):c.136C>T (p.Arg46Trp) rs202202906 0.00001
NM_006789.4(APOBEC2):c.23C>T (p.Ala8Val) rs1184773398 0.00001
NM_006789.4(APOBEC2):c.298G>A (p.Glu100Lys) rs1241781034 0.00001
NM_006789.4(APOBEC2):c.34G>A (p.Glu12Lys) rs775096529 0.00001
NM_006789.4(APOBEC2):c.5C>A (p.Ala2Asp) rs770753227 0.00001
NM_006789.4(APOBEC2):c.150C>G (p.Asn50Lys) rs139783430
NM_006789.4(APOBEC2):c.211T>A (p.Cys71Ser)
NM_006789.4(APOBEC2):c.259C>T (p.Arg87Trp) rs1581991093
NM_006789.4(APOBEC2):c.284C>T (p.Ala95Val)
NM_006789.4(APOBEC2):c.320T>C (p.Ile107Thr)
NM_006789.4(APOBEC2):c.326C>G (p.Pro109Arg)
NM_006789.4(APOBEC2):c.442C>G (p.Leu148Val)
NM_006789.4(APOBEC2):c.499A>C (p.Lys167Gln)
NM_006789.4(APOBEC2):c.505C>G (p.Leu169Val) rs746120000
NM_006789.4(APOBEC2):c.521G>C (p.Cys174Ser)
NM_006789.4(APOBEC2):c.552C>T (p.Phe184=)
NM_006789.4(APOBEC2):c.608A>G (p.Gln203Arg) rs1762881519
NM_006789.4(APOBEC2):c.622A>G (p.Ile208Val) rs2532530944
NM_006789.4(APOBEC2):c.640T>C (p.Tyr214His)
NM_006789.4(APOBEC2):c.646G>A (p.Glu216Lys) rs150558136
NM_006789.4(APOBEC2):c.64G>A (p.Glu22Lys)

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