Variant #0000604149 (NC_000011.9:g.5248212C>T, HBB(NM_000518.4):c.40G>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.5248212C>T
DNA change (hg38) g.5226982C>T
Published as CD 13 GCC>ACC [Ala>Thr]
ISCN -
DB-ID HBB_004140
Variant remarks β-chain variant
Reference IthaNet-3359
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner IthaNet - Petros Kountouris
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-11-08 15:46:08 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBB NM_000518.4 ?/. - c.40G>A Hb Tower Hamlets r.(?) p.(Ala14Thr)