Gene | EGFR |
Variant | missense |
Amino Acid Change | T854A |
DNA Change (Coding Nucleotide) | 2560A>G |
Transcript ID (GRCh37/hg19) | ENST00000275493 |
Codon | 854 |
Exon | 21 |
Genomic Coordinates (GRCh37/hg19) | 7:55259502-55259502 |
COSMIC ID | 28537 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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