LOVD - Variant listings for HGD

About this overview [Show]

Patient data (#0000575)
Patient ID AKU_DB_318
Disease AKU
Reference Soltysova et al. (2021), Russia:Moscow
Remarks Compound heterozygous
# Reported 1
Geographic origin Russia
Patient/Affected_per_Family 1
Families Patients 1
Submitter Alexander Kuzin

Variant data
Allele Parent #2
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
DB-ID AKU_00099
Exon 13
DNA change c.1112A>G
RNA change r.(?)
Protein p.(His371Arg)
Original description H371R
Links rs120074172
Variant remarks missense
Predicted Mutation Effect** Active site disruption, Hexamer disruption
Reference de Bernabe et al. (1999b)
Mutation HOT-SPOT CCC triplet
Allele code AKU_DB_318b
Type substitution
Re-site (-)NcoI
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
Links 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_00042 07 c.457dupG r.(?) p.(Asp153Glyfs*26) D153fs (G152fs) rs397515346 frameshift - Gehrig et al. (1997) CCC triplet AKU_DB_318a insertion - - DNA SEQ exon
+/+ Parent #2 AKU_00099 13 c.1112A>G r.(?) p.(His371Arg) H371R rs120074172 missense Active site disruption, Hexamer disruption de Bernabe et al. (1999b) CCC triplet AKU_DB_318b substitution (-)NcoI - DNA SEQ exon