Gene | KIT |
Variant | missense |
Amino Acid Change | A829P |
DNA Change (Coding Nucleotide) | 2485G>C |
Transcript ID (GRCh37/hg19) | ENST00000288135 |
Codon | 829 |
Exon | 18 |
Genomic Coordinates (GRCh37/hg19) | 4:55602664-55602664 |
COSMIC ID | 13172 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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