Variant #0000250183 (NC_000001.10:g.20974802A>G, PINK1(NM_032409.2):c.1124-196A>G)

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.20974802A>G
DNA change (hg38) g.20648309A>G
Published as PINK1(NM_032409.3):c.1124-196A>G
ISCN -
DB-ID PINK1_000086
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDOST NM_005216.4 -/. - c.*4070T>C r.(=) p.(=)
PINK1 NM_032409.2 -/. - c.1124-196A>G r.(=) p.(=)