RAF1 AMPLIFICATION Detail (hg19) (RAF1)

Information

Genome

Assembly Position
hg19 chr3:12,625,100-12,705,725
hg38 chr3:12,583,601-12,664,226 View the variant detail on this assembly version.
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 164760 OMIM
HGNC 9829 HGNC
Ensembl ENSG00000132155 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 Paclitaxel,Carboplatin,Sorafenib B Predictive Supports Sensitivity/Response Somatic 2 26307133 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

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
RAF1
Genome
hg19
Position
chr3:12,625,100-12,705,725
Variant Type
cnv
Variant (CIViC) (CIViC Variant)
AMPLIFICATION
Transcript 1 (CIViC Variant)
ENST00000251849.4
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/591
Genome browser