Gene | RET |
Variant | missense |
Amino Acid Change | C634W |
DNA Change (Coding Nucleotide) | 1902C>G |
Transcript ID (GRCh37/hg19) | ENST00000355710 |
Codon | 634 |
Exon | 11 |
Genomic Coordinates (GRCh37/hg19) | 10:43609950-43609950 |
COSMIC ID | 975 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
---|