Variant #0000000319 (NC_000011.9:g.5247493_5248849del, HBB(NM_000518.4):c.-598_315+314del)

Chromosome 11
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.5247493_5248849del
Reference Lou et al
DB-ID HBB_000119
Frequency -
Variant remarks Taiwanese
ClassClinical Pathogenic
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBB NM_000518.4 ./. 01-03 c.-598_315+314del r.? p.?