ClinVar Miner

Variants studied for Malignant neoplasm of body of uterus

Coded as:
Minimum submission review status: Collection method:
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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
0 287 0 0 0 287

Gene and significance breakdown #

Total genes and gene combinations: 25
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Gene or gene combination likely pathogenic total
TP53 108 108
PIK3CA 49 49
CTNNB1 28 28
FBXW7 15 15
NRAS 11 11
HRAS, LRRC56 10 10
FGFR2 8 8
ERBB2 6 6
ERBB3 5 5
MTOR 5 5
PPP2R1A 5 5
PTEN 5 5
NFE2L2 4 4
POLE 4 4
SPOP 4 4
BRAF 3 3
MAP2K1 3 3
RAC1 3 3
XPO1 3 3
RHEB 2 2
U2AF1 2 2
KRAS 1 1
MYCN, MYCNOS 1 1
PIK3R1 1 1
SOS1 1 1

Submitter and significance breakdown #

Total submitters: 1
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Submitter likely pathogenic total
Database of Curated Mutations (DoCM) 287 287

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