LOVD - Variant listings for HBG2

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Patient data (#0000597)
Disease Hb variants
Reference (OMIM 0034);dbSNP;SwissVar VAR_003166;Molchanova TP et al.;Glader BE et al.;Priest JR et al.;
Template Protein
Technique Amino
Remarks Hb F-M-Fort Ripley
# Reported 1
Ethnic origin -
Disease Mesh ID C059479
Geographic origin -

Variant data
Allele Unknown
Reported pathogenicity Probably pathogenic
Concluded pathogenicity Unknown
Exon 2
DNA change HBG2:c.277C>T   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.His93Tyr
Re-site -
Frequency -
DB-ID HBG2_00597
HbVar link HbVar

1 entry in HBG2

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 HBG2:c.277C>T - p.His93Tyr - - HBG2_00597 HbVar