Variant #0000928248 (NC_000001.10:g.9780784T>G, NC_000001.10(NM_005026.3):c.1522-16T>G (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.9780784T>G
DNA change (hg38) -
Published as PIK3CD(NM_005026.3):c.1522-16T>G
ISCN -
DB-ID CLSTN1_000050
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) 2.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-07-07 10:10:56 +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.*9782A>C r.(=) p.(=)
PIK3CD NM_005026.3 -?/. - c.1522-16T>G r.(=) p.(=)


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