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KIT V559G
GeneKIT
Variantmissense
Amino Acid ChangeV559G
Transcript ID (GRCh37/hg19)ENST00000288135
Codon559
Germline/Somatic?Somatic
Pertinent Negative In
Tumor TypePrimary Site
See All Pertinent Negatives

Interpretations

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Tier 1
KIT
Variants
KIT V559G
Primary Sites
Unknown
Tumor Types
Gastrointestinal Stromal Tumor
Interpretation

Imatinib

Last updated: 2018-04-18 14:46:32 UTC
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Disclaimer: You assume full responsibility for all risks associated with using this PMKB website. The Englander Institute for Precision Medicine at Weill Cornell Medicine makes no guarantee of the comprehensiveness, reliability or accuracy of the information on this website and assumes no responsibility for errors in the information associated with this web site. Healthcare providers and patients must integrate all clinical and laboratory findings as well as information from a variety of sources before deciding on appropriate clinical care options.

When using PMKB, please cite: Huang et al., JAMIA 2017

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