Variant #0000803669 (NC_000008.10:g.48801117G>A, NM_006904.6:c.4375C>T (PRKDC))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48801117G>A
DNA change (hg38) -
Published as PRKDC(NM_006904.6):c.4375C>T (p.H1459Y)
ISCN -
DB-ID PRKDC_000102 See all 3 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) 0.0003 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 2021-09-17 14:40:49 +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.4375C>T r.(?) p.(His1459Tyr)
PRKDC NM_006904.6 ?/. - c.4375C>T r.(?) p.(His1459Tyr)


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