MTOR p.Leu2137Ile (p.L2137I) Detail (hg38) (MTOR)

Information

Genome

Assembly Position
hg19 chr1:11,184,595-11,184,595 
hg38 chr1:11,124,538-11,124,538

HGVS

Type Transcript Protein
RefSeq NM_004958.3:c.6622C>A NP_004949.1:p.Leu2208Ile
Ensemble ENST00000703140.1:c.6409C>A ENST00000703140.1:p.Leu2137Ile
ENST00000361445.9:c.6622C>A ENST00000361445.9:p.Leu2208Ile
Summary

MGeND

Clinical significance not provided
Variant entry 1
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 601231 OMIM
HGNC 3942 HGNC
Ensembl ENSG00000198793 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
MGeND
Clinical significance Last evaluated Condition Origin Submission ID Submitter Institute Citation Comment Image
not provided 2018/03/08 uterine body cancer somatic MGS000017
(TMGS000052) 		Kohei Miyazono Tokyo University
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg38
Position
chr1:11,124,538-11,124,538
Variant Type
snv
Reference Allele
G
Alternative Allele
T
Genome browser