Variant #0000973602 (NC_000001.10:g.20981976C>T, NM_032409.2:c.*4792C>T (PINK1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.20981976C>T
DNA change (hg38) -
Published as DDOST(NM_005216.5):c.508G>A (p.(Val170Ile), p.V170I)
ISCN -
DB-ID DDOST_000004 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) 0.00077 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDOST NM_005216.4 -?/. - c.559G>A r.(?) p.(Val187Ile)
PINK1 NM_032409.2 -?/. - c.*4792C>T r.(=) p.(=)


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