Variant #0000305004 (NC_000006.11:g.162864412T>C, PARK2(NM_004562.2):c.101A>G)

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.162864412T>C
DNA change (hg38) g.162443380T>C
Published as PARK2(NM_004562.2):c.101A>G (p.Q34R)
ISCN -
DB-ID PARK2_000169
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00291 View details
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     
PARK2 NM_004562.2 -/. - c.101A>G r.(?) p.(Gln34Arg)
PACRG NM_152410.2 -/. - c.-283976T>C r.(?) p.(=)