Gene | BRAF |
Variant | missense |
Amino Acid Change | D594N |
DNA Change (Coding Nucleotide) | 1780G>A |
Transcript ID (GRCh37/hg19) | ENST00000288602 |
Codon | 594 |
Exon | 15 |
Genomic Coordinates (GRCh37/hg19) | 7:140453155-140453155 |
COSMIC ID | 27639 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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Trametinib