Variant #0000272160 (NC_000003.11:g.9786753C>G, NM_016828.2:c.-5218C>G (OGG1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.9786753C>G
DNA change (hg38) g.9745069C>G
Published as BRPF1(NM_001003694.1):c.2982C>G (p.Y994*)
ISCN -
DB-ID BRPF1_000005
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-12 11:19:09 +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.2982C>G r.(?) p.(Tyr994Ter)
CAMK1 NM_003656.4 +?/. - c.*12470G>C r.(=) p.(=)
OGG1 NM_016820.3 +?/. - c.-5218C>G r.(?) p.(=)
OGG1 NM_016828.2 +?/. - c.-5218C>G r.(?) p.(=)


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