ClinVar Miner

Variants studied for Renal cell carcinoma, papillary, 1

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign other total
11 104 486 88 17 1 698

Gene and significance breakdown #

Total genes and gene combinations: 21
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign other total
MET 8 0 476 87 17 0 579
TP53 0 61 0 0 0 0 61
MTOR 1 9 0 1 0 0 11
PIK3CA 0 10 0 0 0 0 10
COMETT, MET 0 0 5 0 0 0 5
NRAS 0 5 0 0 0 0 5
LOC107303340, VHL 1 3 0 0 0 0 4
NFE2L2 0 4 0 0 0 0 4
PTEN 0 4 0 0 0 0 4
ELOC 0 3 0 0 0 0 3
RHEB 0 2 0 0 0 0 2
ASZ1, CAPZA2, CFTR, LOC111365177, LOC111674463, LOC111674464, LOC111674465, LOC111674466, LOC111674476, LOC111674478, LOC113219431, LOC113219432, LOC113219433, LOC113219434, LOC113219439, LOC113219440, LOC113219442, LOC113219443, LOC113219444, LOC113219445, LOC113219446, LOC113219447, LOC116186911, MET, MIR6132, ST7, ST7-OT3, ST7-OT4, WNT2 0 0 1 0 0 0 1
ATM 1 0 0 0 0 0 1
CTNNB1 0 0 0 0 0 1 1
LOC111365177, LOC113219432, MET 0 0 1 0 0 0 1
LOC113219431, LOC113219439, MET 0 0 1 0 0 0 1
MSH2 0 0 1 0 0 0 1
SDHB 0 0 1 0 0 0 1
SF3B1 0 1 0 0 0 0 1
SF3B2 0 1 0 0 0 0 1
VHL 0 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign other total
Invitae 2 0 429 33 0 0 464
Database of Curated Mutations (DoCM) 0 104 0 0 0 0 104
Illumina Clinical Services Laboratory,Illumina 0 0 31 41 13 0 85
Mendelics 2 0 56 18 4 0 80
OMIM 9 0 0 0 0 0 9
CSER _CC_NCGL, University of Washington 0 0 2 0 0 0 2
Institute of Human Genetics,Cologne University 0 0 1 0 0 0 1
Donald Williams Parsons Laboratory,Baylor College of Medicine 0 0 0 0 0 1 1

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