Variant #0000675968 (NC_000001.10:g.9782386C>T, NM_005026.3:c.2319C>T (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.9782386C>T
DNA change (hg38) -
Published as PIK3CD(NM_005026.3):c.2319C>T (p.(Ser773=))
ISCN -
DB-ID CLSTN1_000023
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) 0.01045 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLSTN1 NM_001009566.1 -?/. - c.*8180G>A r.(=) p.(=)
PIK3CD NM_005026.3 -?/. - c.2319C>T r.(?) p.(Ser773=)


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