Variant #0000602821 (NC_000011.9:g.5246908C>T, NM_000518.4:c.364G>A (HBB))

Chromosome 11
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.5246908C>T
DNA change (hg38) g.5225678C>T
Published as [34G>A;364G>A]
ISCN -
DB-ID HBB_000961 See all 41 reported entries
Variant remarks -
Reference data from Globin Gene Server (HbVar-1128), OMIM:var0507, Wajcman H (D-2111-2010), PubMed: Prehu C
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner HbVar - Belinda Giardine and Ross Hardison
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-06-05 12:00:00 +02:00 (CEST)
Date last edited 2019-11-04 20:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBB NM_000518.4 +?/. - c.364G>A Hb O-Tibesti r.(?) p.(Glu122Lys)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.