Variant #0000603857 (NC_000011.9:g.5246878G>T, HBB(NM_000518.4):c.394C>A)

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.5246878G>T
DNA change (hg38) g.5225648G>T
Published as CD 131 CAG>AAG
ISCN -
DB-ID HBB_000987 See all 2 reported entries
Variant remarks β-chain variant
Reference IthaNet-1252
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 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.394C>A Hb Shelby r.(?) p.(Gln132Lys)