LOVD - Variant listings for HBD

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Patient data (#0001395)
Disease Hb variants
Reference (OMIM 0037);dbSNP;SwissVar VAR_003106;Papadakis M et al.;
Template Protein
Technique Amino
Remarks Hb A2-Agrinio
# Reported 1
Ethnic origin -
Disease Mesh ID C097403
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 2
DNA change HBD:c.131A>G   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Glu44Gly
Re-site -
Frequency -
DB-ID HBD_01395
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.131A>G - p.Glu44Gly - - HBD_01395 HbVar