LOVD - Variant listings for HBA2

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Patient data (#0001903)
Disease Hb variants
Reference dbSNP;Barnaby C (E-6612-2010);
Template Protein
Technique Amino
Remarks Hb Codon 14 (TGG>TTG)
# Reported 1
Ethnic origin -
Disease Mesh ID D006455
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 1
DNA change HBA2:c.44G>T   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Trp15Leu
Re-site -
Frequency -
DB-ID HBA2_01641
HbVar link HbVar

1 entry in HBA2

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 1 HBA2:c.44G>T - p.Trp15Leu - - HBA2_01641 HbVar