Variant #0000000589 (NC_000011.9:g.5247905_5247906insT, HBB(NM_000518.4):c.216_217insA)

Chromosome 11
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Insertion
DNA change (genomic) (Relative to hg19 / GRCh37) g.5247905_5247906insT
Reference Chen et al.;(OMIM 0328);dbSNP
DB-ID HBB_000112 See all 2 reported entries
Frequency -
Variant remarks Codons 71/72 (+A)
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 ./. 02 c.216_217insA r.(?) p.(Ser73Lysfs*2)