Variant #0000296761 (NC_000006.11:g.161807855C>G, NM_004562.2:c.1138G>C (PARK2))

Chromosome 6
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.161807855C>G
DNA change (hg38) g.161386823C>G
Published as PARK2(NM_004562.2):c.1138G>C (p.V380L), PRKN(NM_004562.3):c.1138G>C (p.V380L)
ISCN -
DB-ID PARK2_000145 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) 0.16475 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +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.1138G>C r.(?) p.(Val380Leu)
PACRG NM_152410.2 -/. - c.-1340533C>G r.(?) p.(=)


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