LOVD - Variant listings for HBA1

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Patient data (#0000115)
Disease Hb variants
Reference (OMIM 0101);dbSNP;dbSNP;SwissVar VAR_002807;Knuth A et al.;
Template Protein
Technique Amino
Remarks Hb Moabit
# 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 HBA1:c.260T>G   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Leu87Arg
Re-site -
Frequency -
DB-ID HBA1_00115
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.260T>G - p.Leu87Arg - - HBA1_00115 HbVar