Variant #0000795128 (NC_000005.9:g.170814971A>G, NM_002520.6:c.19A>G (NPM1))

Chromosome 5
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.170814971A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID NPM1_000009
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs772365842
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-08-17 08:29:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +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.19A>G r.(?) p.(Met7Val)


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