Variant #0000505030 (NC_000001.10:g.20966418A>G, NM_032409.2:c.709A>G (PINK1))

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.20966418A>G
DNA change (hg38) g.20639925A>G
Published as PINK1(NM_032409.2):c.709A>G (p.M237V), PINK1(NM_032409.3):c.709A>G (p.M237V)
ISCN -
DB-ID PINK1_000093 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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PINK1 NM_032409.2 ?/. - c.709A>G r.(?) p.(Met237Val)


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