Variant #0000000994 (NC_000016.9:g.222938del, HBA2(NM_000517.4):c.27del)

Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.222938del
Reference Tang et al
DB-ID HBA2_000021
Frequency -
Variant remarks Codon9(-C)
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.27del r.(?) p.(Asn10Thrfs*40)