Variant #0000329224 (NC_000003.11:g.9799466T>A, NC_000003.11(NM_016828.2):c.948+966T>A (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.9799466T>A
DNA change (hg38) g.9757782T>A
Published as CAMK1(NM_003656.4):c.977A>T (p.(Glu326Val))
ISCN -
DB-ID CAMK1_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAMK1 NM_003656.4 ?/. - c.977A>T r.(?) p.(Glu326Val)
OGG1 NM_016820.3 ?/. - c.*454T>A r.(=) p.(=)
OGG1 NM_016828.2 ?/. - c.948+966T>A r.(=) p.(=)


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