Variant #0000320522 (NC_000001.10:g.9775972T>A, NM_005026.3:c.436T>A (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.9775972T>A
DNA change (hg38) g.9715914T>A
Published as PIK3CD(NM_005026.3):c.436T>A (p.(Phe146Ile)), PIK3CD(NM_005026.5):c.436T>A (p.F146I)
ISCN -
DB-ID PIK3CD_000003 See all 2 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) 0.00122 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +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.*14594A>T r.(=) p.(=)
PIK3CD NM_005026.3 -?/. - c.436T>A r.(?) p.(Phe146Ile)


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