LOVD - Variant listings for HGD

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Patient data (#0000464)
Patient ID AKU_DB_258
Disease AKU
Reference submitted, United Kingdom (Great Britain):Liverpool
Remarks Compound heterozygous
# Reported 1
Geographic origin United Kingdom
Patient/Affected_per_Family 1
Families Patients 1
Submitter Jeannette Usher

Variant data
Allele Parent #1
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
DB-ID AKU_00208
Exon 08
DNA change c.502G>T
RNA change r.(?)
Protein p.(Glu168*)
Original description G168*
Variant remarks nonsense
Predicted Mutation Effect** -
Reference submitted
Mutation HOT-SPOT -
Allele code AKU_DB_258a
Type substitution
Re-site -
Frequency -
Template DNA
Technique SEQ
Location exon

2 entries in HGD

Path.
Allele Descending
Ascending
DB-ID Descending
Ascending
Exon Descending
Ascending
DNA change Descending
Ascending
RNA change Descending
Ascending
Protein Descending
Ascending
Original description Descending
Ascending
Variant remarks Descending
Ascending
Predicted Mutation Effect** Descending
Ascending
Reference Descending
Ascending
Mutation HOT-SPOT Descending
Ascending
Allele code Descending
Ascending
Type Descending
Ascending
Re-site Descending
Ascending
Frequency Descending
Ascending
Template Descending
Ascending
Technique Descending
Ascending
Location Descending
Ascending
+/+ Parent #1 AKU_00208 08 c.502G>T r.(?) p.(Glu168*) G168* nonsense - submitted - AKU_DB_258a substitution - - DNA SEQ exon
+/+ Parent #2 AKU_00090 12i c.1007-2A>T r.(spl?) p.(Arg336Serfs*5) ivs12-2A>T aberrant splicing (AS)/exon skipping/frameshift - Vilboux et al. (2009) CCC triplet AKU_DB_258b substitution - - DNA SEQ intron