Variant #0000860245 (NC_000006.11:g.161771175C>T, NM_004562.2:c.1354G>A (PARK2))

Chromosome 6
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.161771175C>T
DNA change (hg38) -
Published as PRKN(NM_004562.3):c.1354G>A (p.E452K)
ISCN -
DB-ID PARK2_000205
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PARK2 NM_004562.2 ?/. - c.1354G>A r.(?) p.(Glu452Lys)
PACRG NM_152410.2 ?/. - c.-1377213C>T r.(?) p.(=)


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