LOVD - Variant listings for HBD

About this overview [Show]

Patient data (#0001398)
Disease Hb variants
Reference (OMIM 0009);dbSNP;SwissVar VAR_003110;Ganesan J et al.;Eng LI et al.;Lie-Injo LE et al.;
Template Protein
Technique Amino
Remarks Hb A2-Indonesia
# Reported 1
Ethnic origin -
Disease Mesh ID D006455
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 2
DNA change HBD:c.208G>C   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Gly70Arg
Re-site -
Frequency -
DB-ID HBD_01398
HbVar link HbVar

1 entry in HBD

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 2 HBD:c.208G>C - p.Gly70Arg - - HBD_01398 HbVar