Variant #0000082518 (NC_000005.9:g.177577873del, NC_000005.9(NM_017838.3):c.336+20del (NHP2))

Chromosome 5
Allele Parent #1
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.177577873del
DNA change (hg38) g.178150872del
Published as -
ISCN -
DB-ID NHP2_000008 See all 2 reported entries
Variant remarks all heterozygotes
Reference PubMed: Vulliamy 2008, Journal: Vulliamy 2008
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 3/117 cases
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-10-26 20:36:32 +01:00 (CET)
Date last edited 2020-06-18 11:15:05 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NHP2 NM_017838.3 -/. 3i c.336+20del r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.