Gene | PDGFRA |
Variant | missense |
Amino Acid Change | V561D |
DNA Change (Coding Nucleotide) | 1682T>A |
Transcript ID (GRCh37/hg19) | ENST00000257290 |
Codon | 561 |
Exon | 12 |
Genomic Coordinates (GRCh37/hg19) | 4:55141036-55141036 |
COSMIC ID | 739 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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