Variant #0000000272 (NC_000011.9:g.5254058A>C, HBD(NM_000519.3):c.*136T>G)

Chromosome 11
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.5254058A>C
Reference Xiong et al
DB-ID HBD_000034
Frequency -
Variant remarks +136T>G
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 ./. - c.*136T>G r.spl? p.?