Variant #0000000357 (NC_000011.9:g.5248224_5248225insC, HBB(NM_000518.4):c.27_28insG)

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.5248224_5248225insC
Reference (OMIM 0325);dbSNP
DB-ID HBB_000041
Frequency -
Variant remarks Codons 8/9 (+G);Analysis of a case of rare prenatal diagnosis of severe β-thalassemia
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 c.27_28insG r.(?) p.(Ser10Valfs*14)