Variant #0000505037 (NC_000001.10:g.20977008_20977011dup, PINK1(NM_032409.2):c.1570_1573dup)

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.20977008_20977011dup
DNA change (hg38) g.20650515_20650518dup
Published as PINK1(NM_032409.2):c.1570_1573dupTTAG (p.D525Vfs*38)
ISCN -
DB-ID PINK1_000038 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) Retrieve
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.*1863_*1866dup r.(=) p.(=)
PINK1 NM_032409.2 +/. - c.1570_1573dup r.(?) p.(Asp525ValfsTer38)