Variant #0000976019 (NC_000003.11:g.9787103T>C, NM_016828.2:c.-4868T>C (OGG1))

Chromosome 3
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.9787103T>C
DNA change (hg38) -
Published as BRPF1(NM_001003694.2):c.3069-154T>C
ISCN -
DB-ID BRPF1_000037
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
BRPF1 NM_001003694.1 -?/. - c.3069-154T>C r.(=) p.(=)
CAMK1 NM_003656.4 -?/. - c.*12120A>G r.(=) p.(=)
OGG1 NM_016820.3 -?/. - c.-4868T>C r.(?) p.(=)
OGG1 NM_016828.2 -?/. - c.-4868T>C r.(?) p.(=)


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