LOVD - Variant listings for HBD

About this overview [Show]

Patient data (#0001415)
Disease delta (0 or + unclear) thal
Reference (OMIM 0030);dbSNP;Matsuda M et al.;Nakamura T et al.;Ohta Y et al.;
Template Protein
Technique Amino
Remarks -77 (T->C) delta (0 or + unclear)
# Reported 1
Ethnic origin -
Disease Mesh ID D013789
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 1
DNA change HBD:c.-127T>C   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein -
Re-site -
Frequency -
DB-ID HBD_01415
HbVar link HbVar

1 entry in HBD

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 HBD:c.-127T>C - - - - HBD_01415 HbVar