Variant #0000617464 (NC_000019.9:g.18271391dup, NC_000019.9(NM_005027.3):c.415+18dup (PIK3R2))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18271391dup
DNA change (hg38) g.18160581dup
Published as PIK3R2(NM_005027.3):c.415+18dupT, PIK3R2(NM_005027.4):c.415+18dupT
ISCN -
DB-ID PIK3R2_000026 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) 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIK3R2 NM_005027.3 -/. - c.415+18dup r.(=) p.(=)


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