Gene | RET |
Variant | missense |
Amino Acid Change | C618R |
DNA Change (Coding Nucleotide) | 1852T>C |
Transcript ID (GRCh37/hg19) | ENST00000355710 |
Codon | 618 |
Exon | 10 |
Genomic Coordinates (GRCh37/hg19) | 10:43609096-43609096 |
COSMIC ID | 29803 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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