LOVD - Variant listings for RPS19

About this overview [Show]

Patient data (#0000148)
Patient ID pat1rps1900068
Gender f
Malformations None
Growth Retardation no
Steroid Response yes
Complications -
Variant Origin familial
Reference Draptchinskaia et al (1999) Nat Genet 21, 169-75
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Maternal (confirmed)
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 02
DNA change c.71+3_71+6delGAGT   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.0
Frequency -
DB-ID RPS19_00068
Location Intron 2
Remarks Donor splice site defect
Molecula Mechanisms -
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) 02 c.71+3_71+6delGAGT - p.0 - RPS19_00068 Intron 2 Donor splice site defect - - - - - - - - - -