LOVD - Variant listings for RPS26

About this overview [Show]

Patient data (#0000350)
Patient ID pat1rps2600008
Gender f
Malformations Not Available
Growth Retardation na
Steroid Response na
Complications -
Variant Origin de novo, in patient
Reference Doherty et al (2010) Am J Hum Genet. 2010 Feb 12;86(2) : 222-228
Template DNA
Technique SEQ
Remarks -
# Reported 1

Variant data
Allele Unknown
Reported pathogenicity Pathogenic
Concluded pathogenicity Pathogenic
Exon 02
DNA change c.3+1G>T   (View in UCSC Genome Browser, Ensembl)
RNA change -
Protein p.0?
Frequency -
DB-ID RPS26_00008
Location Intron 1
Remarks Donor splice site defect
Molecula Mechanisms transversion

1 entry in RPS26

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.3+1G>T - p.0? - RPS26_00008 Intron 1 Donor splice site defect transversion