Variant #0001013362 (NC_000001.10:g.9781304G>C, NM_005026.3:c.1809G>C (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.9781304G>C
DNA change (hg38) -
Published as PIK3CD(NM_005026.3):c.1809G>C (p.(=), p.L603=)
ISCN -
DB-ID PIK3CD_000008 See all 3 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) 0.00293 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-10-29 20:49:11 +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     
CLSTN1 NM_001009566.1 -?/. - c.*9262C>G r.(=) p.(=)
PIK3CD NM_005026.3 -?/. - c.1809G>C r.(?) p.(Leu603=)


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