Variant #0000301231 (NC_000008.10:g.48852225C>T, NM_006904.6:c.999G>A (PRKDC))

Chromosome 8
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.48852225C>T
DNA change (hg38) g.47939665C>T
Published as PRKDC(NM_001081640.1):c.999G>A (p.(Met333Ile)), PRKDC(NM_006904.6):c.999G>A (p.M333I)
ISCN -
DB-ID PRKDC_000027 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) 0.03331 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKDC NM_001081640.1 -/. - c.999G>A r.(?) p.(Met333Ile)
PRKDC NM_006904.6 -/. - c.999G>A r.(?) p.(Met333Ile)


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