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BRAF D594N
GeneBRAF
Variantmissense
Amino Acid ChangeD594N
DNA Change (Coding Nucleotide)1780G>A
Transcript ID (GRCh37/hg19)ENST00000288602
Codon594
Exon15
Genomic Coordinates (GRCh37/hg19)7:140453155-140453155
COSMIC ID27639
Germline/Somatic?Somatic
Pertinent Negative In
Tumor TypePrimary Site
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BRAF
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BRAF D594N
Primary Sites
Unknown
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Melanoma
Interpretation

Trametinib

Last updated: 2018-04-06 15:11:17 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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