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Table 1 The scoring system of VIC’s automated step

From: Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants

Evidence (scores)

Strong clinical significance

Potential clinical significance

Benign or likely benign

Uncertain significance

Therapeutic (2/1/0)

2

2/1

0

All other situations

Mutation type (1/0)

1

1

0

Population data (1/0)

1

1

0

Somatic data (2/1/0)

2

2/1

0

Pathway (2/1/0)

2

2/1

0

Germline data (2/1/0)

2

> 1*

1/0

Predictive software (2/1/0)

2

1/0

  1. *The sum of the scores of germline database and predictive software programs