Variant #0000000388 (NC_000011.9:g.5248159C>A, HBB(NM_000518.4):c.92+1G>T)

Individual ID 00000017, 00000738
Chromosome 11
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.5248159C>A
Reference (OMIM 0347);dbSNP;Chen et al.
DB-ID HBB_000058 See all 2 reported entries
Frequency -
Variant remarks IVS-I-1 (G->T)
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.92+1G>T r.spl? p.?



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000016 DNA SEQ-NG-I BCL11A, HBD, HBE1, HBG1, HBG2 19 Qi Ming
0000000737 DNA SEQ-NG-I BCL11A, HBD, HBE1, HBG1, HBG2, HBS1L, MYB 30 Qi Ming