LOVD - Variant listings for RPL5

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Patient data (#0000249)
Patient ID pat1rpl500010
Gender m
Malformations Short stature
Growth Retardation na
Steroid Response no
Complications -
Variant Origin sporadic?(parents not tested)
Reference Quarello et al (2009) Haematologica. 2009 Sep 22. [Epub ahead of print]
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 03
DNA change c.189+1G>A   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.0?
Frequency -
DB-ID RPL5_00010
Location Intron 3
Remarks Donor splice site defect
Molecula Mechanisms transition

1 entry in RPL5

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
+/+ Unknown 03 c.189+1G>A - p.0? - RPL5_00010 Intron 3 Donor splice site defect transition