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.
Legend   How to query  

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.5218G>C r.(?) p.(Glu1740Gln) - VUS g.132230013G>C g.132511169G>C DNAJC13(NM_001329126.1):c.5233G>C (p.E1745Q), DNAJC13(NM_015268.3):c.5218G>C (p.(Glu1740Gln)) - DNAJC13_000057 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. - c.5218G>C r.(?) p.(Glu1740Gln) - likely benign g.132230013G>C g.132511169G>C DNAJC13(NM_001329126.1):c.5233G>C (p.E1745Q), DNAJC13(NM_015268.3):c.5218G>C (p.(Glu1740Gln)) - DNAJC13_000057 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
Legend   How to query