Variant #0000508761 (NC_000001.10:g.9787043A>G, NM_005026.3:c.3074A>G (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.9787043A>G
DNA change (hg38) g.9726985A>G
Published as PIK3CD(NM_005026.3):c.3074A>G (p.E1025G)
ISCN -
DB-ID CLSTN1_000013
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLSTN1 NM_001009566.1 ?/. - c.*3523T>C r.(=) p.(=)
PIK3CD NM_005026.3 ?/. - c.3074A>G r.(?) p.(Glu1025Gly)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.