LOVD - Variant listings for HBG2

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Patient data (#0002093)
Disease Hb variants
Reference Dr. U. Zimmermann ; Dr. H. Frischknecht ; Dr. R. Capalo; Dr. Elisabeth Saller; Dr. F. Dutly; Dr. G. Reinholz ; Dr. Joaquin Bintrup (G-1990-2010);Dr. Elisabeth Kohne; HbVar A-2391-2010;
Template Protein
Technique Amino
Remarks Hb F-Feldkirch
# Reported 1
Ethnic origin -
Disease Mesh ID D006455
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 3
DNA change HBG2:c.317T>A   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Leu106His
Re-site -
Frequency -
DB-ID HBG2_01785
HbVar link HbVar

1 entry in HBG2

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 3 HBG2:c.317T>A - p.Leu106His - - HBG2_01785 HbVar