All variants in the DNM1L gene

Information The variants shown are described using the NM_001278464.1 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

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     
+?/. - c.1376G>T r.(?) p.(Cys459Phe) - likely pathogenic g.32884426G>T g.32731492G>T - - DNM1L_000004 - - - - De novo yes - - 0 - NeuroMeGen
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