LOVD - Variant listings for HBG1

About this overview [Show]

Patient data (#0002318)
Disease Hb variants
Reference Cui J et al.;
Template Protein
Technique Amino
Remarks Hb F-Chori-II
# Reported 1
Ethnic origin -
Disease Mesh ID -
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 1
DNA change HBG1:c.89G>A
RNA change -
Protein p.Gly30Glu
Re-site -
Frequency -
DB-ID HBG1_01991
HbVar link -

1 entry in HBG1

Path.
Allele Descending
Ascending
Exon Descending
Ascending
DNA change Descending
Ascending
RNA change Descending
Ascending
Protein Descending
Ascending
Re-site Descending
Ascending
Frequency Descending
Ascending
DB-ID Descending
Ascending
HbVar link Descending
Ascending
+?/? Unknown 1 HBG1:c.89G>A - p.Gly30Glu - - HBG1_01991 -

  Powered by LOVD v.2.0 Build 38
Enabled modules: mutalyzer, recaptcha, showmaxdbid
©2004-2019 Leiden University Medical Center