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     

Type     

DNA change (genomic) (hg19)     

Published as     

GERP     

Segregation     

DB-ID     

dbSNP ID     

Frequency     

Sources     

Reference     

Variant remarks     

Genetic origin     

Owner     
-/- c.8762A>G p.(His2921Arg) missense_variant - 59/79 benign(0.402) r.(?) tolerated(0.59) subst g.31496398T>C - 2.920 - DMD_000005 rs1800279 - ; clinvar; 25333069;7881286;23757202 - - LOVD
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