Gene | FGFR2 |
Variant | missense |
Amino Acid Change | N549H |
DNA Change (Coding Nucleotide) | 1645A>C |
Transcript ID (GRCh37/hg19) | ENST00000358487 |
Codon | 549 |
Exon | 12 |
Genomic Coordinates (GRCh37/hg19) | 10:123258036-123258036 |
COSMIC ID | 250083 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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