Variant #0000000973 (NC_000016.9:g.213925_281325dup, HBA2(NM_000517.4):c.-8987_*57726dup)

Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Duplication
DNA change (genomic) (Relative to hg19 / GRCh37) g.213925_281325dup
Reference Shang et al
DB-ID HBA1_000007 See all 2 reported entries
Frequency -
Variant remarks 186.8kb dup
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     
HBA2 NM_000517.4 ./. 01-03 c.-8987_*57726dup r.0? p.0?