LOVD - Variant listings for RPS19

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Patient data (#0000124)
Patient ID pat1rps1900053
Gender f
Malformations None
Growth Retardation no
Steroid Response na
Complications -
Variant Origin de novo, in patient
Reference Willig et al (1999) Blood 94, 4294-306
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 04
DNA change c.295_296delGT   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Val99GlyfsX54
Frequency -
DB-ID RPS19_00053
Location -
Remarks Deletion
Molecula Mechanisms slippage
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.295_296delGT - p.Val99GlyfsX54 - RPS19_00053 - Deletion slippage - - - - - - - - -