Variant #0000253162 (NC_000001.10:g.20960385A>T, NM_032409.2:c.344A>T (PINK1))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.20960385A>T
DNA change (hg38) g.20633892A>T
Published as PINK1(NM_032409.2):c.344A>T (p.Q115L), PINK1(NM_032409.3):c.344A>T (p.Q115L)
ISCN -
DB-ID PINK1_000090 See all 2 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) 0.03325 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PINK1 NM_032409.2 -/. - c.344A>T r.(?) p.(Gln115Leu)


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