Gene | EGFR |
Variant | missense |
Amino Acid Change | P546S |
DNA Change (Coding Nucleotide) | 1636C>T |
Transcript ID (GRCh37/hg19) | ENST00000275493 |
Codon | 546 |
Exon | 14 |
Genomic Coordinates (GRCh37/hg19) | 7:55231430-55231430 |
COSMIC ID | 1238072 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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