LOVD - Variant listings for RPL5

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Patient data (#0000277)
Patient ID pat1rpl500026
Gender m
Malformations SGA, short stature, flat thenar
Growth Retardation na
Steroid Response na
Complications -
Variant Origin familial
Reference Cmejla et al (2009) Hum Mutat 30(3), 321-327
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Maternal (confirmed)
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 03
DNA change c.74-1G>A   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.0?
Frequency -
DB-ID RPL5_00026
Location Intron 2
Remarks Acceptor splice site defect
Molecula Mechanisms transition

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
+/+ Maternal (confirmed) 03 c.74-1G>A - p.0? - RPL5_00026 Intron 2 Acceptor splice site defect transition