Variant #0000305676 (NC_000001.10:g.20975602C>T, PINK1(NM_032409.2):c.1366C>T)

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.20975602C>T
DNA change (hg38) g.20649109C>T
Published as PINK1(NM_032409.2):c.1366C>T (p.Q456*)
ISCN -
DB-ID PINK1_000032 See all 3 reported entries
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) 4.0E-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.*3270G>A r.(=) p.(=)
PINK1 NM_032409.2 +/. - c.1366C>T r.(?) p.(Gln456Ter)