ClinVar Miner

Variants studied for cystadenocarcinoma

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
0 225 0 0 0 225

Gene and significance breakdown #

Total genes and gene combinations: 9
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Gene or gene combination likely pathogenic total
TP53 185 185
FBXW7 10 10
PIK3CA 9 9
B2M 5 5
NRAS 5 5
BRAF 3 3
HRAS, LRRC56 3 3
PPP2R1A 3 3
ERBB2 2 2

Submitter and significance breakdown #

Total submitters: 1
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Submitter likely pathogenic total
Database of Curated Mutations (DoCM) 225 225

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