Gene | RET |
Variant | missense |
Amino Acid Change | E511K |
DNA Change (Coding Nucleotide) | 1531G>A |
Transcript ID (GRCh37/hg19) | ENST00000355710 |
Codon | 511 |
Exon | 8 |
Genomic Coordinates (GRCh37/hg19) | 10:43607555-43607555 |
COSMIC ID | 188542 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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