Gene | EGFR |
Variant | missense |
Amino Acid Change | S492R |
DNA Change (Coding Nucleotide) | 1476C>A |
Transcript ID (GRCh37/hg19) | ENST00000275493 |
Codon | 492 |
Exon | 12 |
Genomic Coordinates (GRCh37/hg19) | 7:55228009-55228009 |
COSMIC ID | 236670 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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