LOVD - Variant listings for HBD

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Patient data (#0001403)
Disease Hb variants
Reference (OMIM 0036);dbSNP;SwissVar VAR_014277;Galanello R et al.;
Template Protein
Technique Amino
Remarks Hb A2-Sant' Antioco
# Reported 1
Ethnic origin -
Disease Mesh ID C093040
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 2
DNA change HBD:c.280T>G   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Cys94Gly
Re-site -
Frequency -
DB-ID HBD_01403
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.280T>G - p.Cys94Gly - - HBD_01403 HbVar