Variant #0000602819 (NC_000011.9:g.5246865_5246875del, NM_000518.4:c.397_407del (HBB))

Chromosome 11
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.5246865_5246875del
DNA change (hg38) g.5225635_5225645del
Published as codons 128/129 (-4, -GCTG; +5, +CCACA) codons 132-135 (-11, -AAAGTGGTGGC) Dominant inclusion body beta-thal trait
ISCN -
DB-ID HBB_004091 See all 2 reported entries
Variant remarks -
Reference data from Globin Gene Server (HbVar-963), OMIM:var0520, PubMed: Weatherall, PubMed: Thein
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner HbVar - Belinda Giardine and Ross Hardison
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-06-05 12:00:00 +02:00 (CEST)
Date last edited 2019-11-05 20:12:48 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBB NM_000518.4 +?/. 3 c.397_407del - r.(?) p.(Lys133Trpfs*4)


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