Variant #0000610214 (NC_000006.11:g.161969969G>A, NM_004562.2:c.1000C>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.161969969G>A
DNA change (hg38) g.161548937G>A
Published as PARK2(NM_004562.2):c.1000C>T (p.R334C), PRKN(NM_004562.3):c.1000C>T (p.R334C)
ISCN -
DB-ID PARK2_000047 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) 0.00245 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 2019-12-04 15:24:38 +01:00 (CET)
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     
PARK2 NM_004562.2 ?/. - c.1000C>T r.(?) p.(Arg334Cys)
PACRG NM_152410.2 ?/. - c.-1178419G>A r.(?) p.(=)


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