Variant #0000269883 (NC_000023.10:g.135741283_135741287del, NM_000074.2:c.495_499del (CD40LG))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.135741283_135741287del
DNA change (hg38) g.136659124_136659128del
Published as CD40LG(NM_000074.2):c.495_499delACAAG (p.Q166Tfs*33)
ISCN -
DB-ID CD40LG_000011
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-21 10:14:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD40LG NM_000074.2 +/. - c.495_499del r.(?) p.(Gln166ThrfsTer33)


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