Variant #0000566615 (NC_000019.9:g.18266970G>A, NM_005027.3:c.281G>A (PIK3R2))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.18266970G>A
DNA change (hg38) g.18156160G>A
Published as PIK3R2(NM_005027.4):c.281G>A (p.R94H)
ISCN -
DB-ID MAST3_000008
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIK3R2 NM_005027.3 ?/. - c.281G>A r.(?) p.(Arg94His)
MAST3 NM_015016.1 ?/. - c.*6434G>A r.(=) p.(=)


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