Variant #0000603515 (NC_000011.9:g.5248184T>G, HBB(NM_000518.4):c.68A>C)

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.5248184T>G
DNA change (hg38) g.5226954T>G
Published as CD 22 GAA>GCA (Hb G-Hsin Chu , Hb G-Saskatoon , Hb G-Taegu)
ISCN -
DB-ID HBB_000718 See all 8 reported entries
Variant remarks β-chain variant
Reference IthaNet-876
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner IthaNet - Petros Kountouris
Database submission license No license selected
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBB NM_000518.4 ?/. - c.68A>C Hb G-Coushatta r.(?) p.(Glu23Ala)