Variant #0000717123 (NC_000001.10:g.20980247T>C, PINK1(NM_032409.2):c.*3063T>C)

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.20980247T>C
DNA change (hg38) -
Published as DDOST(NM_005216.4):c.866A>G (p.Y289C)
ISCN -
DB-ID DDOST_000016
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDOST NM_005216.4 ?/. - c.866A>G r.(?) p.(Tyr289Cys)
PINK1 NM_032409.2 ?/. - c.*3063T>C r.(=) p.(=)