LOVD - Variant listings for RPS19

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Patient data (#0000055)
Patient ID pat1rps1900021
Gender m
Malformations Not available
Growth Retardation na
Steroid Response na
Complications -
Variant Origin familial
Reference Campagnoli et al (2008) Hum Mutat Apr 15
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Maternal (confirmed)
Reported pathogenicity Pathogenic
Concluded pathogenicity Probably pathogenic
Exon 03
DNA change c.156G>C   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Trp52Cys
Frequency -
DB-ID RPS19_00021
Location -
Remarks Missense mutation
Molecula Mechanisms transversion
Functional_Classific -
mRNA_Expression -
Protein_Expression -
Protein_Localization -
rRNA_Metabolism -
Protein_Synthesis -
Cell_Growth -
Functional_Remarks -
Functional_Reference -

1 entry in RPS19

Path.
Allele Descending
Ascending
Exon Descending
Ascending
DNA change Descending
Ascending
RNA change Descending
Ascending
Protein Descending
Ascending
Frequency Descending
Ascending
DB-ID Descending
Ascending
Location Descending
Ascending
Remarks Descending
Ascending
Molecula Mechanisms Descending
Ascending
Functional_Classific Descending
Ascending
mRNA_Expression Descending
Ascending
Protein_Expression Descending
Ascending
Protein_Localization Descending
Ascending
rRNA_Metabolism Descending
Ascending
Protein_Synthesis Descending
Ascending
Cell_Growth Descending
Ascending
Functional_Remarks Descending
Ascending
Functional_Reference Descending
Ascending
+/+? Maternal (confirmed) 03 c.156G>C - p.Trp52Cys - RPS19_00021 - Missense mutation transversion - - - - - - - - -