Variant #0001000308 (NC_000012.11:g.6954849G>A, NM_002075.2:c.799G>A (GNB3))

Chromosome 12
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.6954849G>A
DNA change (hg38) -
Published as GNB3(NM_002075.2):c.799G>A (p.(Glu267Lys))
ISCN -
DB-ID CDCA3_000017
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) 0.00013 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
GNB3 NM_002075.2 -?/. - c.799G>A r.(?) p.(Glu267Lys)
CDCA3 NM_031299.4 -?/. - c.*3358C>T r.(=) p.(=)


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