LOVD - Variant listings for RPL11

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Patient data (#0000325)
Patient ID pat2rpl1100021
Gender f
Malformations Left thumb: additional short phalanx
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 04
DNA change c.396+1G>A   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.0?
Frequency -
DB-ID RPL11_00021
Location Intron 4
Remarks Donor splice site defect
Molecula Mechanisms transition

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.396+1G>A - p.0? - RPL11_00021 Intron 4 Donor splice site defect transition