ClinVar Miner

List of variants in gene DMD reported as uncertain significance for Becker muscular dystrophy

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_000109.4(DMD):c.1294G>A (p.Glu432Lys) rs189143447
NM_000109.4(DMD):c.1700T>C (p.Leu567Pro) rs370644567
NM_000109.4(DMD):c.3320T>C (p.Ile1107Thr) rs748123444
NM_000109.4(DMD):c.5465G>T (p.Arg1822Ile) rs369055628
NM_000109.4(DMD):c.679C>A (p.Leu227Ile) rs200177107
NM_004006.2(DMD):c.10058A>C (p.His3353Pro) rs1569423551
NM_004006.2(DMD):c.1687C>T (p.Arg563Cys) rs145739725
NM_004006.2(DMD):c.1897A>T (p.Asn633Tyr) rs757047592
NM_004006.2(DMD):c.2330T>C (p.Leu777Pro) rs794727226
NM_004006.2(DMD):c.2912A>T (p.Asp971Val) rs762154042
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.9352G>T (p.Ala3118Ser) rs200928985
NM_004006.2(DMD):c.9580A>C (p.Ile3194Leu) rs181517869
NM_004006.2(DMD):c.960+9A>G rs886038537
NM_004006.3(DMD):c.1000T>A rs1280415176
NM_004006.3(DMD):c.265-438T>C rs1459975890
NM_004006.3(DMD):c.295A>G (p.Ile99Val) rs149428656
NM_004006.3(DMD):c.5999A>T (p.Tyr2000Phe) rs1603630432
NM_004006.3(DMD):c.8704C>T (p.Arg2902Trp) rs1188233243
NM_004006.3(DMD):c.8762A>G (p.His2921Arg) rs1800279

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