LOVD - Variant listings for HBA1

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Patient data (#0000037)
Disease Hb variants
Reference (OMIM 0124);dbSNP;dbSNP;SwissVar VAR_002744;Bardakdjian-Michau J et al.;
Template Protein
Technique Amino
Remarks Hb Reims
# Reported 1
Ethnic origin -
Disease Mesh ID C063954
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 1
DNA change HBA1:c.71A>G   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Glu24Gly
Re-site -
Frequency -
DB-ID HBA1_00037
HbVar link HbVar

1 entry in HBA1

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 HBA1:c.71A>G - p.Glu24Gly - - HBA1_00037 HbVar