LOVD - Variant listings for RPL5

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Patient data (#0000257)
Patient ID pat1rpl500016
Gender m
Malformations Micrognathia, hypertelorism, soft cleft palate, triphalangeal right thumb, widened webbed spaced between first and second toes, hypospadias
Growth Retardation na
Steroid Response na
Complications -
Variant Origin sporadic?(parents not tested)
Reference Gazda et al (2008) Am J Hum Genet 83(6), 769-80
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 02
DNA change c.46_47insA   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Tyr16X
Frequency -
DB-ID RPL5_00016
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.46_47insA - p.Tyr16X - RPL5_00016 - Insertion slippage