ClinVar Miner

Variants from ClinGen TP53 Variant Curation Expert Panel, ClinGen

Location: United States  Primary collection method: curation
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
18 11 27 58 5 119

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
TP53 18 11 27 58 5 119

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic likely pathogenic uncertain significance likely benign benign total
Li-Fraumeni syndrome 14 10 11 22 5 62
Li-Fraumeni syndrome 1 4 1 16 36 0 57

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