Gene | ALK |
Variant | missense |
Amino Acid Change | C1156Y |
DNA Change (Coding Nucleotide) | 3467G>A |
Transcript ID (GRCh37/hg19) | ENST00000389048 |
Codon | 1156 |
Exon | 22 |
Genomic Coordinates (GRCh37/hg19) | 2:29445258-29445258 |
COSMIC ID | 99136 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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