Gene | PDGFRA |
Variant | missense |
Amino Acid Change | N848K |
DNA Change (Coding Nucleotide) | 2544C>A |
Transcript ID (GRCh37/hg19) | ENST00000257290 |
Codon | 848 |
Exon | 18 |
Genomic Coordinates (GRCh37/hg19) | 4:55152112-55152112 |
COSMIC ID | 28052 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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