Variant #0001032257 (NC_000001.10:g.9777122G>A, NM_005026.3:c.886G>A (PIK3CD))

Chromosome 1
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.9777122G>A
DNA change (hg38) -
Published as PIK3CD(NM_005026.5):c.886G>A (p.(Val296Ile))
ISCN -
DB-ID CLSTN1_000064
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) 0.00714 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     
CLSTN1 NM_001009566.1 -?/. - c.*13444C>T r.(=) p.(=)
PIK3CD NM_005026.3 -?/. - c.886G>A r.(?) p.(Val296Ile)


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