Variant #0000000389 (NC_000011.9:g.5248159C>A, HBB(NM_000518.4):c.92+1G>T)

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.5248159C>A
Reference (OMIM 0347);dbSNP;Kazazian HH Jr et al.;
DB-ID HBB_000058 See all 2 reported entries
Frequency -
Variant remarks IVS-I-1 (G->T); AG^GTTGGT->AGTTTGGT beta0
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     
HBB NM_000518.4 ./. 01 c.92+1G>T r.spl? p.?