LOVD - Variant listings for RPL5

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Patient data (#0000246)
Patient ID pat1rpl500007
Gender m
Malformations Facial dysmorphisms, strabism
Growth Retardation na
Steroid Response yes
Complications -
Variant Origin de novo, in patient
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 02
DNA change c.39_40insT   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Lys14X
Frequency -
DB-ID RPL5_00007
Location -
Remarks Insertion
Molecula Mechanisms slippage

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 02 c.39_40insT - p.Lys14X - RPL5_00007 - Insertion slippage