Variant #0001039434 (NC_000012.11:g.6952186C>T, NM_002075.2:c.149C>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.6952186C>T
DNA change (hg38) -
Published as GNB3(NM_002075.4):c.149C>T (p.(Thr50Met))
ISCN -
DB-ID CDCA3_000018
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 2025-05-05 21:14:00 +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.149C>T r.(?) p.(Thr50Met)
LEPREL2 NM_014262.3 ?/. - c.*3561C>T r.(=) p.(=)
CDCA3 NM_031299.4 ?/. - c.*6021G>A r.(=) p.(=)


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