All transcript variants in gene DMD

This database is one of the gene variant databases from the Leiden Muscular Dystrophy pages.
NOTE: for MLPA-detected deletion/duplication variants we use a probe-based HGVS description, for the exon-based description check the "Published as" column.
Information The variants shown are described using the NM_004006.2 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
+/. 1i_17i c.(-182_59)_(2085_2226)dup pathogenic (recessive) r.(32_2168dup) p.(fs*) g.(32536191_32563359)_(33038290_33229611)dup g.(32518074_32545242)_(33020173_33211494)dup c.(31+1_32-1)_(2168+1_2169-1)dup - DMD_020217 - Jorge ESHG2006 P1191 - - Germline - - - 0 - Johan den Dunnen
+/. 1i_17i c.(-182_59)_(2085_2226)dup pathogenic (recessive) r.? p.? g.(32536191_32563359)_(33038290_33229611)dup g.(32518074_32545242)_(33020173_33211494)dup dup ex2-17; c.(31+1_32-1)_(2168+1_2169-1)dup - DMD_020217 - PubMed: Wang 2017 - - Germline/De novo (untested) - - - 0 - Johan den Dunnen
+/. 1i_17i c.(-182_59)_(2085_2226)dup pathogenic (recessive) r.? p.(fs*) g.(32536191_32563359)_(33038290_33229611)dup g.(32518074_32545242)_(33020173_33211494)dup dup ex2-17; c.(31+1_32-1)_(2168+1_2169-1)dup - DMD_020217 - Ling 2019, submitted - - Germline/De novo (untested) - - - 0 - Chao Ling
+/. 1i_17i c.(-182_59)_(2085_2226)dup pathogenic (recessive) r.? p.(fs*) g.(32536191_32563359)_(33038290_33229611)dup g.(32518074_32545242)_(33020173_33211494)dup dup ex2-17; c.(31+1_32-1)_(2168+1_2169-1)dup - DMD_020217 - Ling 2019, submitted - - Germline/De novo (untested) - - - 0 - Chao Ling
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