Gene | KIT |
Variant | insertion |
Amino Acid Change | Y503_F504insSA |
DNA Change (Coding Nucleotide) | 1507_1508insCTGCCT |
Transcript ID (GRCh37/hg19) | ENST00000288135 |
Codon | 503-504 |
Exon | 9 |
Genomic Coordinates (GRCh37/hg19) | 4:55592183-55592184 |
COSMIC ID | 219786 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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