LOVD - Variant listings for HBD

About this overview [Show]

Patient data (#0001874)
Disease Hb variants
Reference dbSNP;Francina A (E-3974-2010);
Template DNA
Technique SEQ
Remarks Hb A2-Lyon
# 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.120G>C   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Gln40His
Re-site -
Frequency -
DB-ID HBD_01616
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.120G>C - p.Gln40His - - HBD_01616 HbVar