Variant #0000000993 (NC_000016.9:g.1_282199dup, HBA2(NM_000517.4):c.-222911_*58600dup)

Chromosome 16
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Type Duplication
DNA change (genomic) (Relative to hg19 / GRCh37) g.1_282199dup
Reference Hu et al
DB-ID HBA2_000040 See all 2 reported entries
Frequency -
Variant remarks αααα282.1
ClassClinical Uncertain significance
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 ./. 01-03 c.-222911_*58600dup r.0? p.0?