Variant #0000339000 (NC_000003.11:g.9787588C>T, NM_016828.2:c.-4383C>T (OGG1))

Chromosome 3
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.9787588C>T
DNA change (hg38) g.9745904C>T
Published as BRPF1(NM_001003694.2):c.3298C>T (p.R1100*)
ISCN -
DB-ID BRPF1_000007 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 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRPF1 NM_001003694.1 ?/. - c.3298C>T r.(?) p.(Arg1100Ter)
CAMK1 NM_003656.4 ?/. - c.*11635G>A r.(=) p.(=)
OGG1 NM_016820.3 ?/. - c.-4383C>T r.(?) p.(=)
OGG1 NM_016828.2 ?/. - c.-4383C>T r.(?) p.(=)


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