Variant #0000000263 (NC_000011.9:g.5255640_5255642delCTC, HBD(NM_000519.3):c.22_24delGAG)

Chromosome 11
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.5255640_5255642delCTC
Reference Zhong et al
DB-ID HBD_000037
Frequency -
Variant remarks Codon8(-GAG)
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     
HBD NM_000519.3 ./. 01 c.22_24delGAG r.(?) p.(Glu8del)