KRAS AMPLIFICATION Detail (hg38) (KRAS)

Information

Genome

Assembly Position
hg19 chr12:25,362,365-25,403,737 View the variant detail on this assembly version.
hg38 chr12:25,209,431-25,250,803
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 190070 OMIM
HGNC 6407 HGNC
Ensembl ENSG00000133703 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
skin melanoma Carboplatin,Sorafenib,Docetaxel B Predictive Supports Sensitivity/Response N/A 2 26307133 Detail
endometrial cancer B Prognostic Supports Poor Outcome Somatic 3 23099803 Detail
melanoma Vemurafenib D Predictive Supports Resistance Somatic 2 24265155 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
Retrospective analysis of somatic mutations and copy number changes in 119 patients treated with car... CIViC Evidence Detail
In this study, KRAS gain (KRAS/CEP12q ratio >1 and <2) or amplification (ratio >2) was detected in 3... CIViC Evidence Detail
In vitro studies of M229 (a human melanoma cell line) endogenously expressing wildtype KRAS and BRAF... 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
KRAS
Genome
hg38
Position
chr12:25,209,431-25,250,803
Variant Type
cnv
Variant (CIViC) (CIViC Variant)
AMPLIFICATION
Transcript 1 (CIViC Variant)
ENST00000256078.4
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/592
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