Variant #0000654146 (NC_000001.10:g.9787030G>A, NM_005026.3:c.3061G>A (PIK3CD))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.9787030G>A
DNA change (hg38) g.9726972G>A
Published as PIK3CD(NM_001350234.2):c.3058G>A (p.E1020K), PIK3CD(NM_005026.3):c.3061G>A (p.E1021K), PIK3CD(NM_005026.5):c.3061G>A (p.E1021K)
ISCN -
DB-ID PIK3CD_000010 See all 5 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) 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +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.*3536C>T r.(=) p.(=)
PIK3CD NM_005026.3 +/. - c.3061G>A r.(?) p.(Glu1021Lys)


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