Variant #0000000380 (NC_000011.9:g.5248167_5248168insG, HBB(NM_000518.4):c.84_85insC)

Chromosome 11
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Insertion
DNA change (genomic) (Relative to hg19 / GRCh37) g.5248167_5248168insG
Reference (OMIM 0342);dbSNP;Chen et al.
DB-ID HBB_000053 See all 2 reported entries
Frequency -
Variant remarks Codons 27/28 (+C)
ClassClinical Pathogenic
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     
HBB NM_000518.4 ./. 01 c.84_85insC r.(?) p.(Leu29Profs*16)