ClinVar Miner

List of variants in gene DMD reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP
NM_004006.2(DMD):c.*1005T>G rs905224596
NM_004006.2(DMD):c.*1049T>C rs1057515860
NM_004006.2(DMD):c.*1049_*1052delTGAT rs71860126
NM_004006.2(DMD):c.*1049_*1052dupTGAT rs71860126
NM_004006.2(DMD):c.*1161_*1164dupAACT rs1057515859
NM_004006.2(DMD):c.*1339G>C rs1057515858
NM_004006.2(DMD):c.*1349T>G rs764825924
NM_004006.2(DMD):c.*1425_*1428dupTAAA rs1057515857
NM_004006.2(DMD):c.*1448_*1449insAAGA rs1057515856
NM_004006.2(DMD):c.*1455C>A rs191747923
NM_004006.2(DMD):c.*1588_*1591dupTGTT rs771242421
NM_004006.2(DMD):c.*1731A>C rs3198427
NM_004006.2(DMD):c.*1758_*1761delTTCA rs751300992
NM_004006.2(DMD):c.*192G>A rs1057515866
NM_004006.2(DMD):c.*2031_*2034dupAATT rs1057515855
NM_004006.2(DMD):c.*2234_*2237dupAAGT rs202154420
NM_004006.2(DMD):c.*2234_*2238dupAAGTT rs1057515854
NM_004006.2(DMD):c.*2314T>C rs1057515853
NM_004006.2(DMD):c.*237T>C rs955717911
NM_004006.2(DMD):c.*473_*476dupCACA rs386416845
NM_004006.2(DMD):c.*475_*476dupCA rs386416845
NM_004006.2(DMD):c.*477T>C rs764294071
NM_004006.2(DMD):c.*489_*492dupCACA rs763028610
NM_004006.2(DMD):c.*491_*492delCA rs763028610
NM_004006.2(DMD):c.*704C>T rs1057515863
NM_004006.2(DMD):c.*807_*810dupGTCA rs1057515862
NM_004006.2(DMD):c.*952_*956dupAAGTA rs745368386
NM_004006.2(DMD):c.-123T>C rs760595740
NM_004006.2(DMD):c.-155C>T rs960566728
NM_004006.2(DMD):c.-75G>A rs778938887
NM_004006.2(DMD):c.10146C>G (p.Thr3382=) rs766427132
NM_004006.2(DMD):c.10262+1G>A rs145603325
NM_004006.2(DMD):c.10789C>T (p.Leu3597=) rs1800281
NM_004006.2(DMD):c.1249G>C (p.Glu417Gln) rs1057515877
NM_004006.2(DMD):c.1616G>A (p.Arg539Gln) rs1057515876
NM_004006.2(DMD):c.1809G>A (p.Leu603=) rs192176661
NM_004006.2(DMD):c.2146G>C (p.Val716Leu) rs886043081
NM_004006.2(DMD):c.2210G>A (p.Arg737His) rs773358704
NM_004006.2(DMD):c.2245A>G (p.Ile749Val) rs771803281
NM_004006.2(DMD):c.2939G>A (p.Gly980Glu) rs1057515875
NM_004006.2(DMD):c.3169A>G (p.Ile1057Val) rs1057515874
NM_004006.2(DMD):c.3450G>T (p.Glu1150Asp) rs142967431
NM_004006.2(DMD):c.3603+8A>G rs193249735
NM_004006.2(DMD):c.3666T>C (p.Asn1222=) rs373281760
NM_004006.2(DMD):c.3816G>C (p.Leu1272Phe) rs760733415
NM_004006.2(DMD):c.3921+12A>G rs760373690
NM_004006.2(DMD):c.3936G>C (p.Leu1312Phe) rs377156960
NM_004006.2(DMD):c.3951G>A (p.Glu1317=) rs199643655
NM_004006.2(DMD):c.4744G>A (p.Val1582Ile) rs398123965
NM_004006.2(DMD):c.4845+4A>T rs368357171
NM_004006.2(DMD):c.5047A>C (p.Thr1683Pro) rs1057515873
NM_004006.2(DMD):c.5263C>T (p.Pro1755Ser) rs1057515872
NM_004006.2(DMD):c.530+7A>T rs72470523
NM_004006.2(DMD):c.5361C>T (p.Asn1787=) rs1057515871
NM_004006.2(DMD):c.5586+9G>A rs200025478
NM_004006.2(DMD):c.5620G>A (p.Glu1874Lys) rs142441725
NM_004006.2(DMD):c.5741A>G (p.Glu1914Gly) rs985546923
NM_004006.2(DMD):c.5923-4C>G rs780118536
NM_004006.2(DMD):c.5933G>T (p.Arg1978Leu) rs148135406
NM_004006.2(DMD):c.5964C>T (p.Asp1988=) rs1057515869
NM_004006.2(DMD):c.6455T>C (p.Ile2152Thr) rs767681834
NM_004006.2(DMD):c.6471T>A (p.Thr2157=) rs377080659
NM_004006.2(DMD):c.6912+7C>T rs779161941
NM_004006.2(DMD):c.7151C>A (p.Ser2384Tyr) rs185706283
NM_004006.2(DMD):c.7200+9G>A rs748786108
NM_004006.2(DMD):c.8509G>A (p.Asp2837Asn) rs965718917
NM_004006.2(DMD):c.8571T>C (p.Thr2857=) rs72466570
NM_004006.2(DMD):c.8888T>C (p.Val2963Ala) rs1057515867
NM_004006.2(DMD):c.9324T>G (p.Thr3108=) rs766256437
NM_004006.2(DMD):c.9486G>A (p.Glu3162=) rs370724251
NM_004006.2(DMD):c.9564-5A>G rs201390145

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