Variant #0000298758 (NC_000003.11:g.9792781G>A, NM_016828.2:c.290G>A (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.9792781G>A
DNA change (hg38) g.9751097G>A
Published as OGG1(NM_016821.3):c.290G>A (p.R97H)
ISCN -
DB-ID OGG1_000019
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRPF1 NM_001003694.1 -?/. - c.*3748G>A r.(=) p.(=)
CAMK1 NM_003656.4 -?/. - c.*6442C>T r.(=) p.(=)
OGG1 NM_016820.3 -?/. - c.290G>A r.(?) p.(Arg97His)
OGG1 NM_016828.2 -?/. - c.290G>A r.(?) p.(Arg97His)


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