chr1:11127037:G>T Detail (hg38) (MTOR)

Information

Genome

Assembly Position
hg19 chr1:11,187,094-11,187,094 View the variant detail on this assembly version.
hg38 chr1:11,127,037-11,127,037

HGVS

Type Transcript Protein
RefSeq NM_004958.3:c.6324C>A NP_004949.1:p.Phe2108Leu
Ensemble ENST00000361445.9:c.6324C>A ENST00000361445.9:p.Phe2108Leu
ENST00000703140.1:c.6111C>A ENST00000703140.1:p.Phe2037Leu
Summary

MGeND

Clinical significance
Variant entry
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 COSM4439845 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
thyroid gland carcinoma Everolimus C Predictive Supports Resistance Somatic 5 25295501 Detail
breast cancer Sirolimus D Predictive Supports Resistance Somatic 4 27279227 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
The pretreatment tumor contained a somatic nonsense mutation (Q1178*) in the tumor-suppressor gene T... CIViC Evidence Detail
MCF-7 breast cancer cell line was exposed to mTOR inhibitors AZD8055 or rapamycin until resistance d... CIViC Evidence Detail

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
chr1:11,127,037-11,127,037
Variant Type
snv
Reference Allele
G
Alternative Allele
T
Variant (CIViC) (CIViC Variant)
F2108L
Transcript 1 (CIViC Variant)
ENST00000361445.4
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/470
Genome browser