Variant #0000603849 (NC_000011.9:g.5246884C>G, HBB(NM_000518.4):c.388G>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.5246884C>G
DNA change (hg38) g.5225654C>G
Published as CD 129 GCC>CCC
ISCN -
DB-ID HBB_000981 See all 9 reported entries
Variant remarks β-chain variant
Reference IthaNet-1244
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
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.388G>C Hb Crete r.(?) p.(Ala130Pro)