Gene Name HGNC ID COSMIC_MutID Primary sitePrimary histology AA-Mutation Mutation Type Genomic PositionFATHMM predictionFATHMM scoreLiterature evidence
ACTN1163COSM39799, central_nervous_systemgliomap.S145LSubstitution - Missense14:68910036-68910036, PATHOGENIC0.9987618772396
ACTN1163COSM1580424, haematopoietic_and_lymphoid_tissuelymphoid_neoplasmp.A811VSubstitution - Missense14:68877170-68877170, PATHOGENIC0.9869123292937
ACTN1163COSM1580425, haematopoietic_and_lymphoid_tissuelymphoid_neoplasmp.T709ISubstitution - Missense14:68880817-68880817, PATHOGENIC0.95923292937