LOVD - Variant listings for RPL5

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Patient data (#0000291)
Patient ID pat1rpl500036
Gender f
Malformations Triphalangeal thumb
Growth Retardation na
Steroid Response na
Complications -
Variant Origin de novo, in patient
Reference U. Ramenghi, Dept. Pediatrics Università di Torino
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 03
DNA change c.91delT   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Tyr31MetfsX7
Frequency -
DB-ID RPL5_00036
Location -
Remarks Deletion
Molecula Mechanisms -

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.91delT - p.Tyr31MetfsX7 - RPL5_00036 - Deletion -