Variant #0000000323 (NC_000011.9:g.5157109_5361649dup, HBB(NM_000518.4):c.-113398_*89719dup)

Chromosome 11
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Type Duplication
DNA change (genomic) (Relative to hg19 / GRCh37) g.5157109_5361649dup
Reference Shang et al
DB-ID HBD_000031 See all 4 reported entries
Frequency -
Variant remarks 204k dup
ClassClinical Uncertain significance
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.-113398_*89719dup r.0? p.0?