ClinVar Miner

List of variants reported as uncertain significance for Becker muscular dystrophy

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 17
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HGVS dbSNP
NM_003098.2(SNTA1):c.620G>A (p.Arg207Gln) rs771180054
NM_004006.2(DMD):c.10058A>C (p.His3353Pro) rs1569423551
NM_004006.2(DMD):c.1318G>A (p.Glu440Lys) rs189143447
NM_004006.2(DMD):c.1687C>T (p.Arg563Cys) rs145739725
NM_004006.2(DMD):c.2330T>C (p.Leu777Pro) rs794727226
NM_004006.2(DMD):c.2912A>T (p.Asp971Val)
NM_004006.2(DMD):c.295A>G (p.Ile99Val) rs149428656
NM_004006.2(DMD):c.3344T>C (p.Ile1115Thr) rs748123444
NM_004006.2(DMD):c.5489G>T (p.Arg1830Ile) rs369055628
NM_004006.2(DMD):c.5869C>T (p.Arg1957Trp) rs755477994
NM_004006.2(DMD):c.6409G>C (p.Glu2137Gln) rs1023328955
NM_004006.2(DMD):c.6839G>A (p.Ser2280Asn) rs1060502614
NM_004006.2(DMD):c.703C>A (p.Leu235Ile) rs200177107
NM_004006.2(DMD):c.8762A>G (p.His2921Arg) rs1800279
NM_004006.2(DMD):c.9352G>T (p.Ala3118Ser) rs200928985
NM_004006.2(DMD):c.9580A>C (p.Ile3194Leu) rs181517869
NM_004572.3(PKP2):c.1468C>T (p.Arg490Trp) rs149930872

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