Variant #0000170723 (NC_000016.9:g.219817_(223755_224074)del)

Individual ID 00104761
Chromosome 16
Allele Parent #2
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.219817_(223755_224074)del
DNA change (hg38) -
Published as -α4.2
ISCN -
DB-ID HBA2_000000 See all 3 reported entries
Variant remarks -
Reference PubMed: He 2017, Journal: He 2017
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 1/951 individuals
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Baosheng Zhu
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-05-24 09:01:29 +02:00 (CEST)
Date last edited 2017-05-24 09:08:43 +02:00 (CEST)
Options




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000105235 DNA SEQ-NG - - HBA1, HBA2, HBB 2 Baosheng Zhu


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