LOVD - Variant listings for HBA1

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Patient data (#0000047)
Disease Hb variants
Reference (OMIM 0055);dbSNP;dbSNP;dbSNP;dbSNP;SwissVar VAR_002752;Shih MC et al.;De Marco EV et al.;
Template Protein
Technique Amino
Remarks Hb Prato
# Reported 1
Ethnic origin -
Disease Mesh ID C076578
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 2
DNA change HBA1:c.[96G>C or 96G>T ]
RNA change -
Protein p.Arg32Ser
Re-site -
Frequency -
DB-ID HBA1_00047
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 2 HBA1:c.[96G>C or 96G>T ] - p.Arg32Ser - - HBA1_00047 HbVar