Gene | KIT |
Variant | missense |
Amino Acid Change | V559I |
DNA Change (Coding Nucleotide) | 1675G>A |
Transcript ID (GRCh37/hg19) | ENST00000288135 |
Codon | 559 |
Exon | 11 |
Genomic Coordinates (GRCh37/hg19) | 4:55593609-55593609 |
COSMIC ID | 1251 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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