Variant #0000305024 (NC_000006.11:g.162206909G>A, NM_004562.2:c.766C>T (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.162206909G>A
DNA change (hg38) g.161785877G>A
Published as PARK2(NM_004562.2):c.766C>T (p.R256C), PRKN(NM_004562.3):c.766C>T (p.R256C)
ISCN -
DB-ID PARK2_000032 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) 0.00043 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     
PARK2 NM_004562.2 ?/. - c.766C>T r.(?) p.(Arg256Cys)
PACRG NM_152410.2 ?/. - c.-941479G>A r.(?) p.(=)


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