Variant #0000527930 (NC_000006.11:g.162394341C>T, NM_004562.2:c.727G>A (PARK2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.162394341C>T
DNA change (hg38) g.161973309C>T
Published as PARK2(NM_004562.2):c.727G>A (p.D243N), PRKN(NM_004562.3):c.727G>A (p.D243N)
ISCN -
DB-ID PARK2_000186 See all 2 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) 0.00029 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 2019-07-18 18:22:55 +02:00 (CEST)
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.727G>A r.(?) p.(Asp243Asn)
PACRG NM_152410.2 -?/. - c.-754047C>T r.(?) p.(=)


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