Gene | RET |
Variant | missense |
Amino Acid Change | S649L |
DNA Change (Coding Nucleotide) | 1946C>T |
Transcript ID (GRCh37/hg19) | ENST00000355710 |
Codon | 649 |
Exon | 11 |
Genomic Coordinates (GRCh37/hg19) | 10:43609994-43609994 |
COSMIC ID | 4170226 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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