Variant #0000566624 (NC_000019.9:g.18285896C>T, NM_005027.3:c.*5792C>T (PIK3R2))

Chromosome 19
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.18285896C>T
DNA change (hg38) g.18175086C>T
Published as IFI30(NM_006332.3):c.179C>T (p.(Pro60Leu))
ISCN -
DB-ID PIK3R2_000032
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) 0.00233 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIK3R2 NM_005027.3 -?/. - c.*5792C>T r.(=) p.(=)
IFI30 NM_006332.3 -?/. - c.179C>T r.(?) p.(Pro60Leu)


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