Variant #0001054226 (NC_000012.11:g.6952813C>T, NM_002075.2:c.448C>T (GNB3))

Chromosome 12
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.6952813C>T
DNA change (hg38) -
Published as GNB3(NM_002075.4):c.448C>T (p.(Arg150Cys))
ISCN -
DB-ID CDCA3_000020
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) 2.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
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.448C>T r.(?) p.(Arg150Cys)
LEPREL2 NM_014262.3 ?/. - c.*4188C>T r.(=) p.(=)
CDCA3 NM_031299.4 ?/. - c.*5394G>A r.(=) p.(=)


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