ClinVar Miner

Variants studied for bladder transitional cell carcinoma

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

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 total
0 276 0 0 0 276

Gene and significance breakdown #

Total genes and gene combinations: 27
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Gene or gene combination likely pathogenic total
TP53 119 119
PIK3CA 32 32
CTNNB1 21 21
BRAF 11 11
HRAS, LRRC56 11 11
ERBB2 10 10
FBXW7 10 10
NFE2L2 8 8
NRAS 8 8
CDKN2A 5 5
ERBB3 5 5
IDH1 5 5
CREBBP 4 4
FGFR3 3 3
MAP2K1 3 3
SF3B1 3 3
CNOT9 2 2
EP300 2 2
FGFR1 2 2
MTOR 2 2
RHEB 2 2
RXRA 2 2
U2AF1 2 2
AKT1 1 1
KRAS 1 1
MAPK1 1 1
PTEN 1 1

Submitter and significance breakdown #

Total submitters: 1
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Submitter likely pathogenic total
Database of Curated Mutations (DoCM) 276 276

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