LOVD - Variant listings for RPL11

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Patient data (#0000311)
Patient ID pat1rpl1100011
Gender f
Malformations Short stature
Growth Retardation na
Steroid Response no
Complications -
Variant Origin familial
Reference Quarello et al (2009) Haematologica. 2009 Sep 22. [Epub ahead of print]
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Paternal (confirmed)
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 06
DNA change c.508-2A>G   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.0?
Frequency -
DB-ID RPL11_00011
Location Intron 5
Remarks Acceptor splice site defect
Molecula Mechanisms transition

1 entry in RPL11

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
+/+ Paternal (confirmed) 06 c.508-2A>G - p.0? - RPL11_00011 Intron 5 Acceptor splice site defect transition