Variant #0000861235 (NC_000008.10:g.48852225C>T, NM_006904.6:c.999G>A (PRKDC))

Chromosome 8
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.48852225C>T
DNA change (hg38) -
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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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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