Variant #0000525169 (NC_000005.9:g.170837540_170837541insTCTG, NM_002520.6:c.856_857insTCTG (NPM1))

Chromosome 5
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.170837540_170837541insTCTG
DNA change (hg38) g.171410536_171410537insTCTG
Published as NPM1(NM_002520.6):c.856_857insTCTG (p.D286Vfs*2)
ISCN -
DB-ID NPM1_000006
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 09:20:54 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPM1 NM_002520.6 ?/. - c.856_857insTCTG r.(?) p.(Asp286ValfsTer2)


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