ClinVar Miner

Variants studied for carcinosarcoma of the corpus uteri

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
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 total
0 174 0 0 0 174

Gene and significance breakdown #

Total genes and gene combinations: 12
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Gene or gene combination likely pathogenic total
TP53 111 111
PIK3CA 22 22
FBXW7 15 15
ERBB3 5 5
PPP2R1A 5 5
PTEN 5 5
HRAS, LRRC56 3 3
POLE 3 3
U2AF1 2 2
ERBB2 1 1
FGFR2 1 1
PIK3R1 1 1

Submitter and significance breakdown #

Total submitters: 1
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Submitter likely pathogenic total
Database of Curated Mutations (DoCM) 174 174

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