Variant #0000001000 (NC_000016.9:g.222963G>T, HBA2(NM_000517.4):c.52G>T)

Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.222963G>T
Reference Yang et al
DB-ID HBA2_000038 See all 2 reported entries
Frequency -
Variant remarks Hb Dapu
ClassClinical Pathogenic
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     
HBA2 NM_000517.4 ./. 01 c.52G>T r.(?) p.(Val18Phe)