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. 2015 Feb 19;8:46. doi: 10.1186/s13104-015-0983-5

Table 1.

RBM10 mutations

Phenotype Mutation effect Mutation Exon Protein Reference
NSCLC Missense 2 E4K Imielinski et al. [10]
NSCLC Missense 2 R6H Imielinski et al. [10]
TARP syndrome Frameshift c.159delC 3 p.Lys54SerfsX80 Gripp et al. [7]
NSCLC Nonsense 3 E67 Imielinski et al. [10]
TARP syndrome c.448C>T 4 p.Gln150X Johnston et al. [8]
NSCLC Nonsense 5 R157fs Imielinski et al. [10]
NSCLC Nonsense 7 Y206 Imielinski et al. [10]
NSCLC Nonsense 8 R230 Imielinski et al. [10]
TARP syndrome c.724+2T>C 8 Johnston et al. [8]
NSCLC Missense 10 1316F Imielinski et al. [10]
TARP syndrome Nonsense c.1235G>A 12 p.Trp412X Johnston et al. [6]
NSCLC Missense 16 Y580F Imielinski et al. [10]
NSCLC Splice site 17 Y596 Imielinski et al. [10]
Pancreatic neoplasm Frameshift c.1817-1818insA 17 p.E606EfsX37 Furukawa et al. [9]
TARP syndrome Frameshift c.1893-1894insA 17 p.Pro632ThrfsX41 Johnston et al. [6]
TARP syndrome Deletion aa651-889 18-23 Wang et al. [3]
NSCLC Missense 18 R685L Imielnski et al. [10]
TARP syndrome c.2176C>T 20 p.Arg726X Johnston et al. [8]
NSCLC Nonsense 21 E810 Imielinski et al. [10]
NSCLC Splice site 22 V846 Imielinski et al. [10]