Gene | RET |
Variant | missense |
Amino Acid Change | C634F |
DNA Change (Coding Nucleotide) | 1901G>T |
Transcript ID (GRCh37/hg19) | ENST00000355710 |
Codon | 634 |
Exon | 11 |
Genomic Coordinates (GRCh37/hg19) | 10:43609949-43609949 |
COSMIC ID | 1237919 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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