ClinVar Miner

Variants from Laboratory of Translational Genomics, National Cancer Institute

Location: United States  Primary collection method: not provided
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 not provided total
0 0 0 0 0 42 42

Gene and significance breakdown #

Total genes and gene combinations: 8
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Gene or gene combination not provided total
TP53 9 9
ERBB2 7 7
PIK3CA 7 7
KRAS 6 6
FGFR3 5 5
EGFR 4 4
GATA3 3 3
BRAF 1 1

Condition and significance breakdown #

Total conditions: 4
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Condition not provided total
Familial cancer of breast 15 15
Sarcoma 13 13
Endometrial carcinoma 8 8
Ovarian neoplasm 6 6

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