Variant #0000525170 (NC_000005.9:g.170837547_170837548insCGTG, NM_002520.6:c.863_864insCGTG (NPM1))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.170837547_170837548insCGTG
DNA change (hg38) g.171410543_171410544insCGTG
Published as NPM1(NM_002520.6):c.863_864insCGTG (p.W288Cfs*12)
ISCN -
DB-ID NPM1_000007
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-18 09:20:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPM1 NM_002520.6 +/. - c.863_864insCGTG r.(?) p.(Trp288CysfsTer12)


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