Overview

Variant ID 608
Entrez Gene ID 2475
Gene MTOR (GeneCards)
Location hg19 1:11210266-11210266
hg38 1:11150209-11150209
Disease Focal Cortical Dysplasias (view all the variants in this disease)
Method Sanger
Mutation(HGVS format) NC_000001.10:g.11210266 A>C (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 1456
Amino acid changes in protein W > G
Position in cDNA 4487
Changes in cDNA T > G
mRNA accession NM_004958.3
mRNA length 8733
Reference length 249250621

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.0415
CADD Raw score (version 1.3) 3.191787 (Deleterious)
FATHMM raw prediction score 0.99834 (Tolerated)
SIFT score 0.035 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 0.97 (Tolerated)
PROVEAN score -0.79 (Tolerated)
MetaSVM score -1.034 (Tolerated)
MetaLR score 0.019 (Tolerated)
MCAP score 0.033 (Deleterious)
FitCons score 0.732 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.31
PhyloP score based on multiple alignment of 100 vertebrates 7.645
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 15.278
Deleterious probability by DeFine 0.9563 (Deleterious)
Entrez Gene ID 2475 (NCBI Gene)
Official Gene Symbol MTOR (GeneCards)
Number of variants in MTOR in this database 21 (view all the variants)
Full name mechanistic target of rapamycin kinase
Band 1p36.22
Other IDs Vega: OTTHUMG00000002001
OMIM: 601231
HGNC: HGNC:3942
Ensembl: ENSG00000198793
Other names SKS, FRAP, FRAP1, FRAP2, RAFT1, RAPT1
Summary The protein encoded by this gene belongs to a family of phosphatidylinositol kinase-related kinases. These kinases mediate cellular responses to stresses such as DNA damage and nutrient deprivation. This protein acts as the target for the cell-cycle arrest and immunosuppressive effects of the FKBP12-rapamycin complex. The ANGPTL7 gene is located in an intron of this gene. [provided by RefSeq, Sep 2008]

Individual #1

Individual ID 25878179.01 (view all the variants in this individual)
Pubmed ID 25878179
Whose mosaic mutation Male Patient  
Origin of mosaic mutation in patients de novo
Phenotype 3  
Disease Focal Cortical Dysplasias (view all the variants in this disease)
OMIM ID 607341

Publication #1: 25878179

Pubmed ID 25878179
Title Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR.
Journal Neurology
Publication date 2015.05
Disease Focal Cortical Dysplasias
Number of cases Male cases: 1;