LOVD - Variant listings for RPS19

About this overview [Show]

Patient data (#0000067)
Patient ID pat1rps1900025
Gender na
Malformations Not available
Growth Retardation na
Steroid Response na
Complications -
Variant Origin sporadic?(parents not tested)
Reference Gazda et al (2004) Br J Haematol 127, 105-13
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Probably pathogenic
Exon 04
DNA change c.176C>T   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Ser59Phe
Frequency -
DB-ID RPS19_00025
Location -
Remarks Missense mutation
Molecula Mechanisms transition
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
+/+? Unknown 04 c.176C>T - p.Ser59Phe - RPS19_00025 - Missense mutation transition - - - - - - - - -