All transcript variants in gene DCX

MSeqDR-LSDB: Mitochondrial Disease LSDB
Information The variants shown are described using the transcript reference sequence.

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

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     

Type     

DNA change (genomic) (hg19)     

Published as     

GERP     

Segregation     

DB-ID     

dbSNP ID     

Frequency     

Sources     

Reference     

Variant remarks     

Genetic origin     

Owner     
./. - - c.280A>G - - - - - - g.110653347T>C - - - DCX_000003 - - ; clinvar; - - - LOVD
./. - - c.315_316insTAC - - - - - - g.110653311_110653312insGTA - - - DCX_000002 - - ; clinvar; - - - LOVD
./. - - c.339_340insC - - - - - - g.110653287_110653288insG - - - DCX_000001 - - ; clinvar; - - - LOVD
./. - - c.528del - - - - - - g.110644395del - - - DCX_000004 - - ; clinvar; - - - LOVD
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Variations Associated with Mitochondrial Diseases Gene

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium