All variants in the PRKN gene

Information The variants shown are described using the NM_004562.2 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     

DNA change (genomic) (hg38)     

Published as     

Reference     

DB-ID     

dbSNP ID     

Frequency     

Variant remarks     

Owner     
+/. 12 c.1321T>C - r.(?) p.(Cys441Arg) Pathogenic g.161350176A>G - Shen-Yang Lim et al.(2021): https://www.neurology-asia.org/articles/neuroasia-2021-26(1)-161.pdf PRKN_000001 rs778305273 - - Nur Aisyah Athirah
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