Variant #0000001062 (NC_000016.9:g.227055G>C, HBA1(NM_000558.3):c.223G>C)

Individual ID 00000233, 00000331, 00001944
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.227055G>C
Reference Hu et al
DB-ID HBA1_000042
Frequency -
Variant remarks Hb Q-Thailand
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     
HBA1 NM_000558.3 ./. 02 c.223G>C r.(?) p.(Asp75His)



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000232 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2 49 Qi Ming
0000000330 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2, HBS1L 56 Qi Ming
0000001943 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2 50 Qi Ming