MET - Renal cell carcinoma, papillary type 1
This test is available for the following conditions:
- Conditions > Renal / Nephrological > Renal cell carcinoma
- Conditions > Oncogenetics > Renal cell carcinoma
This product is also part of the following panels:
- Comprehensive preconception carrier test panel¹
- Hearing impairment panel (including GJB2)
- Hereditary cancer panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- panel hereditary renalcancer (SDHA, SDHB, SDHC, SDHD, SDHAF2, VHL, PTEN, FLCN, MET, FH, BAP1)
- Short stature/skeletal dysplasia panel with genome wide CNV analysis
Turnaround time
Complete analysis & Targeted analysis: 3 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
164860
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA