Gene | VHL |
Variant | missense |
Amino Acid Change | L188Q |
DNA Change (Coding Nucleotide) | 563T>A |
Transcript ID (GRCh37/hg19) | ENST00000256474 |
Codon | 188 |
Exon | 3 |
Genomic Coordinates (GRCh37/hg19) | 3:10191570-10191570 |
COSMIC ID | 17800 |
Germline/Somatic? | Somatic |
Tumor Type | Primary Site |
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