LOVD - Variant listings for RPL5

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Patient data (#0000281)
Patient ID pat1rpl500029
Gender m
Malformations SGA, flat thenar, short stature
Growth Retardation na
Steroid Response yes
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 08
DNA change c.854C>T   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.Ala285Val
Frequency -
DB-ID RPL5_00029
Location -
Remarks Missense mutation
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) 08 c.854C>T - p.Ala285Val - RPL5_00029 - Missense mutation transition