Table 1 Number of mutations* in each tumor sample.

From: Exome sequencing identifies novel somatic variants in African American esophageal squamous cell carcinoma

Tumor

2 or more variant caller (> 50DP, 5 > VAF)

#SNV < 1%AFR

# of InDel

Total coding mutations

T14

3460

1940

878

T6

3339

1239

804

T5

2716

1243

686

T1

2152

1033

588

T7

1663

956

491

T16

125

9

49

T15

80

1

44

T8

93

629

29

T9

22

0

6

T19

13

0

5

  1. *Mutations called by two or more algorithms, filtered for rare (< 1% MAF) African population frequency, and sorted by somatic nonsynonymous coding mutations.
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