Variant #0000678397 (NC_000008.10:g.48868509C>A, NC_000008.10(NM_006904.6):c.325-1G>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.48868509C>A
DNA change (hg38) -
Published as PRKDC(NM_006904.6):c.325-1G>T
ISCN -
DB-ID MCM4_000025
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKDC NM_001081640.1 ?/. - c.325-1G>T r.spl? p.?
MCM4 NM_005914.3 ?/. - c.-5196C>A r.(?) p.(=)
PRKDC NM_006904.6 ?/. - c.325-1G>T r.spl? p.?


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