Variant #0000001017 (NC_000016.9:g.223597T>C, HBA2(NM_000517.4):c.427T>C)

Individual ID 00000554, 00001296
Chromosome 16
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.223597T>C
Reference Fang et al
DB-ID HBA2_000019
Frequency -
Variant remarks Hb Constant Spring
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     
HBA2 NM_000517.4 ./. 03 c.427T>C r.(?) p.(*143Glnext*31)



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000553 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2, HBS1L, MYB 50 Qi Ming
0000001295 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2, HBS1L, MYB 56 Qi Ming