Variant #0000293765 (NC_000019.9:g.18280032C>T, NM_005027.3:c.2115C>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.18280032C>T
DNA change (hg38) g.18169222C>T
Published as PIK3R2(NM_005027.4):c.2115C>T (p.N705=)
ISCN -
DB-ID PIK3R2_000021
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.2115C>T r.(?) p.(Asn705=)
IFI30 NM_006332.3 -?/. - c.-4620C>T r.(?) p.(=)


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