LOVD - Variant listings for HBA2

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Patient data (#0000291)
Disease Hb variants
Reference (OMIM 0016);dbSNP;dbSNP;SwissVar VAR_002745;Codrington JF et al.;Blackwell RQ et al.;Boyer SH et al.;
Template Protein
Technique Amino
Remarks Hb Chad
# Reported 1
Ethnic origin -
Disease Mesh ID C040492
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 1
DNA change HBA2:c.70G>A   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Glu24Lys
Re-site -
Frequency -
DB-ID HBA2_00291
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.70G>A - p.Glu24Lys - - HBA2_00291 HbVar