View all transcript variants in gene DMD

Information The variants shown are described using the NM_004006.2 transcript reference sequence.

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Effect     

AscendingDNA change (cDNA)     

Protein     

GVS function     

Position     

Exon     

PolyPhen     

RNA change     

SIFT     

Chr     

Allele     

Type     

DNA change (genomic) (hg19)     

Published as     

GERP     

Segregation     

DB-ID     

MSCV     

dbSNP ID     

Frequency     

Sources     

Reference     

Variant remarks     

Genetic origin     

Owner     
+/+ c.3631G>T p.(Glu1211*) stop_gained - 27/79 - r.(?) - X Unknown subst g.32466728C>A - 4.660 - DMD_000004 MSCV_0003642 rs267606771 - ; clinvar; 9410897 - - -
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