ClinVar Miner

List of variants in gene MAGEA3 reported as uncertain significance

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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_005362.4(MAGEA3):c.83C>T (p.Ala28Val) rs782605651 0.00073
NM_005362.4(MAGEA3):c.835G>A (p.Val279Ile) rs1361909824 0.00018
NM_005362.4(MAGEA3):c.895A>G (p.Ile299Val) rs1556827180 0.00009
NM_005362.3(MAGEA3):c.418G>A rs782278365 0.00008
NM_005362.4(MAGEA3):c.374G>A (p.Arg125Gln) rs140660790 0.00005
NM_005362.4(MAGEA3):c.760A>G (p.Asn254Asp) rs1556826927 0.00004
NM_005362.4(MAGEA3):c.889C>G (p.Pro297Ala) rs1421845987 0.00003
NM_005362.4(MAGEA3):c.901T>C (p.Tyr301His) rs1931778312 0.00003
NM_005362.4(MAGEA3):c.329G>A (p.Ser110Asn) rs782483422 0.00002
NM_005362.4(MAGEA3):c.933G>T (p.Glu311Asp) rs1556827244 0.00002
NM_005362.4(MAGEA3):c.880A>G (p.Ser294Gly) rs149795670 0.00001
NM_005362.4(MAGEA3):c.892C>A (p.His298Asn) rs1556827170 0.00001
NM_005362.4(MAGEA3):c.100G>C (p.Glu34Gln) rs1931723321
NM_005362.4(MAGEA3):c.142G>C (p.Val48Leu)
NM_005362.4(MAGEA3):c.171G>C (p.Glu57Asp)
NM_005362.4(MAGEA3):c.189G>C (p.Gln63His)
NM_005362.4(MAGEA3):c.206C>A (p.Ser69Tyr) rs1931730670
NM_005362.4(MAGEA3):c.336G>C (p.Lys112Asn) rs2124945229
NM_005362.4(MAGEA3):c.349G>A (p.Val117Ile) rs2521483198
NM_005362.4(MAGEA3):c.370T>C (p.Tyr124His)
NM_005362.4(MAGEA3):c.456C>G (p.Ser152Arg)
NM_005362.4(MAGEA3):c.501G>A (p.Met167Ile)
NM_005362.4(MAGEA3):c.502G>A (p.Glu168Lys)
NM_005362.4(MAGEA3):c.521A>G (p.His174Arg) rs782412538
NM_005362.4(MAGEA3):c.697G>A (p.Gly233Arg) rs149483923
NM_005362.4(MAGEA3):c.707A>G (p.Asp236Gly)
NM_005362.4(MAGEA3):c.725C>T (p.Pro242Leu) rs2521489922
NM_005362.4(MAGEA3):c.755A>G (p.Gln252Arg)
NM_005362.4(MAGEA3):c.776G>A (p.Arg259Gln)
NM_005362.4(MAGEA3):c.868A>T (p.Met290Leu)
NM_005362.4(MAGEA3):c.934G>A (p.Gly312Arg)

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