Variant #0000531793 (NC_000007.13:g.2974203T>C, NM_032415.4:c.1402A>G (CARD11))

Chromosome 7
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.2974203T>C
DNA change (hg38) g.2934569T>C
Published as CARD11(NM_001324281.1):c.1402A>G (p.R468G), CARD11(NM_032415.7):c.1402A>G (p.(Arg468Gly))
ISCN -
DB-ID CARD11_000017 See all 2 reported entries
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CARD11 NM_032415.4 ?/. - c.1402A>G r.(?) p.(Arg468Gly)


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