LOVD - Variant listings for RPL11

About this overview [Show]

Patient data (#0000327)
Patient ID pat1rpl1100023
Gender f
Malformations SGA, flat thenar, bifid thumb
Growth Retardation na
Steroid Response yes
Complications -
Variant Origin sporadic?(parents not tested)
Reference Cmejla et al (2009) Hum Mutat 30(3), 321-327
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 04
DNA change c.357T>G   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Tyr119X
Frequency -
DB-ID RPL11_00023
Location -
Remarks Nonsense mutation
Molecula Mechanisms transversion

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
+/+ Unknown 04 c.357T>G - p.Tyr119X - RPL11_00023 - Nonsense mutation transversion