KIT AMPLIFICATION Detail (hg19) (KIT)

Information

Genome

Assembly Position
hg19 chr4:55,524,085-55,606,881
hg38 chr4:54,657,918-54,740,715 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 164920 OMIM
HGNC 6342 HGNC
Ensembl ENSG00000157404 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
mucosal melanoma Imatinib B Predictive Supports Resistance N/A 3 23775962 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
Phase 2 trial in metastatic mucosal, acral or chronically sun-damaged melanoma. Twenty-five patients... 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
KIT
Genome
hg19
Position
chr4:55,524,085-55,606,881
Variant Type
cnv
Variant (CIViC) (CIViC Variant)
AMPLIFICATION
Transcript 1 (CIViC Variant)
ENST00000288135.5
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/586
Genome browser