Variant #0000689680 (NC_000006.11:g.162206914T>C, NM_004562.2:c.761A>G (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.162206914T>C
DNA change (hg38) -
Published as PRKN(NM_004562.2):c.761A>G (p.N254S)
ISCN -
DB-ID PARK2_000203
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) 2.0E-5 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2020-10-03 10:19:50 +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.761A>G r.(?) p.(Asn254Ser)
PACRG NM_152410.2 -?/. - c.-941474T>C r.(?) p.(=)


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