Variant #0000603912 (NC_000011.9:g.5246835T>C, HBB(NM_000518.4):c.437A>G)

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.5246835T>C
DNA change (hg38) g.5225605T>C
Published as CD 145 TAT>TGT
ISCN -
DB-ID HBB_001022 See all 2 reported entries
Variant remarks β-chain variant
Reference IthaNet-1310
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner IthaNet - Petros Kountouris
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBB NM_000518.4 ?/. - c.437A>G Hb Rainier r.(?) p.(Tyr146Cys)