LOVD - Variant listings for HBB

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Patient data (#0000677)
Disease Hb variants
Reference (OMIM 0451);dbSNP;Langdown JV et al.;
Template Protein
Technique Amino
Remarks Hb Tyne
# Reported 1
Disease Mesh ID C091966

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 1
DNA change HBB:c.16C>T   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Pro6Ser
DB-ID HBB_00677
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.16C>T - p.Pro6Ser HBB_00677 HbVar