LOVD - Variant listings for HBB

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Patient data (#0000676)
Disease Hb variants
Reference (OMIM 0296);dbSNP;SwissVar VAR_002861;Wilson CI et al.;
Template Protein
Technique Amino
Remarks Hb Warwickshire
# Reported 1
Disease Mesh ID C043183

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 1
DNA change HBB:c.17C>G   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Pro6Arg
DB-ID HBB_00676
HbVar link HbVar

1 entry in HBB

Path.
Allele Descending
Ascending
Exon Descending
Ascending
DNA change Descending
Ascending
RNA change Descending
Ascending
Protein Descending
Ascending
DB-ID Descending
Ascending
HbVar link Descending
Ascending
+?/? Unknown 1 HBB:c.17C>G - p.Pro6Arg HBB_00676 HbVar