Variant #0000603574 (NC_000011.9:g.5247996_5247998del^5247993_5247995del, NM_000518.4:c.124_126del^127_129del (HBB))

Chromosome 11
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.5247996_5247998del^5247993_5247995del
DNA change (hg38) g.5226766_5226768del^5226763_5226765del
Published as CD 41 (-TTC) or CD 42 (-TTT), 124_126delTTC | 127_129delTTT
ISCN -
DB-ID HBB_001061 See all 2 reported entries
Variant remarks β-chain variant
Reference IthaNet-945
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner IthaNet - Petros Kountouris
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-11-08 15:46:08 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBB NM_000518.4 ?/. - c.124_126del^127_129del Hb Bruxelles r.(?) p.(Phe43del)


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