Variant #0000001052 (NC_000016.9:g.226799G>T, HBA1(NM_000558.3):c.84G>T)

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.226799G>T
Reference Yao et al
DB-ID HBA1_000030
Frequency -
Variant remarks Codon28(G>T)
ClassClinical Uncertain significance
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBA1 NM_000558.3 ./. 01 c.84G>T r.(?) p.(Glu28Asp)