Variant #0000001064 (NC_000016.9:g.227069delC, HBA1(NM_000558.3):c.237delC)

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.227069delC
Reference Shang et al
DB-ID HBA1_000032
Frequency -
Variant remarks Codon 79(-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     
HBA1 NM_000558.3 ./. 02 c.237delC r.(?) p.(Asn79Lysfs*6)