Variant #0000962940 (NC_000003.11:g.9788916dup, NM_016828.2:c.-3055dup (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.9788916dup
DNA change (hg38) -
Published as BRPF1(NM_001003694.2):c.3546dupG (p.L1183Afs*33)
ISCN -
DB-ID BRPF1_000033
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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRPF1 NM_001003694.1 ?/. - c.3546dup r.(?) p.(Leu1183Alafs*33)
CAMK1 NM_003656.4 ?/. - c.*10307dup r.(?) p.(=)
OGG1 NM_016820.3 ?/. - c.-3055dup r.(?) p.(=)
OGG1 NM_016828.2 ?/. - c.-3055dup r.(?) p.(=)


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