All variants in the DNAJC13 gene

A Parkinson's disease Mutation Database
Information The variants shown are described using the NM_015268.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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.4385G>A r.(?) p.(Arg1462His) - likely benign g.132218621G>A g.132499777G>A DNAJC13(NM_015268.4):c.4385G>A (p.R1462H) - DNAJC13_000022 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_VUmc
-/. - c.4385G>A r.(?) p.(Arg1462His) - benign g.132218621G>A g.132499777G>A DNAJC13(NM_015268.4):c.4385G>A (p.R1462H) - DNAJC13_000022 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
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