Variant #0000606021 (NC_000001.10:g.9777117C>T, NM_005026.3:c.881C>T (PIK3CD))

Chromosome 1
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.9777117C>T
DNA change (hg38) g.9717059C>T
Published as PIK3CD(NM_005026.5):c.881C>T (p.P294L)
ISCN -
DB-ID CLSTN1_000015
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLSTN1 NM_001009566.1 ?/. - c.*13449G>A r.(=) p.(=)
PIK3CD NM_005026.3 ?/. - c.881C>T r.(?) p.(Pro294Leu)


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