LOVD - Variant listings for HGD

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Patient data (#0000182)
Patient ID AKU_VIL_29
Disease AKU
Reference Vilboux et al. (2009), Slovakia (Slovak Republic):Bratislava
Remarks Compound heterozygous
# Reported 1
Geographic origin USA
Patient/Affected_per_Family 1
Families Patients 1
Submitter Andrea Zatkova

Variant data
Allele Parent #2
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
DB-ID AKU_00003
Exon 01
DNA change c.11T>A
RNA change r.(?)
Protein p.(Leu4*)
Original description L4*
Variant remarks nonsense
Predicted Mutation Effect** -
Reference Phornphutkul et al. (2002)
Mutation HOT-SPOT -
Allele code AKU_VIL_29a
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 #2 AKU_00003 01 c.11T>A r.(?) p.(Leu4*) L4* nonsense - Phornphutkul et al. (2002) - AKU_VIL_29a substitution - - DNA SEQ exon
+/+ Parent #1 AKU_00097 13 c.1102A>G r.(?) p.(Met368Val) M368V missense Hexamer disruption de Bernabe et al. (1998) - AKU_VIL_29b substitution (+)BtsIMutI, HpyCH4III, Tsp45I, TspRI - DNA SEQ exon