Variant #0000000588 (NC_000011.9:g.5247905_5247906insT, HBB(NM_000518.4):c.216_217insA)

Individual ID 00000713, 00000745, 00001260
Chromosome 11
Allele Both (homozygous)
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 (OMIM 0328);dbSNP;Chen et al.
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)



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000712 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2, MYB 49 Qi Ming
0000000744 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2 49 Qi Ming
0000001259 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2 48 Qi Ming