Table 2 In silico analysis of 13 BRCA1 variants of unknown significance/putative variants affecting splicing

From: Functional characterization of BRCA1 gene variants by mini-gene splicing assay

NT change (HGVS)

NT change (BIC)

Location

SpliceSiteFinder (0100)

MaxEntScan (012)

NNSplice (01)

GeneSplicer (015)]

Human Splicing Finder (0100)

Effect observed in mini-gene assay

RNA change (HGVS)

5-Tier splicing classification a

c.-19-22_-19-21dupAT

101−21insAT

Intron 1

NI NI

SA: 4.90 4.90 (0%)

NI NI

NI NI

SD: 71.51 71.51 (0%)

No aberration

r.[=]

Class 2

c.80+1G>A

199+1G>A

Intron 2

SD: 91.49 NI (−100%)

SD: 10.65 NI (−100%)

SD: 1.00 NI (−100%)

SD: 1.93 NI (−100%)

SD: 95.25 NI (−100%)

Skipping of exon 2

r.[ 19_80del]

Class 5

c.132C>T

251C>T

Exon 3

SD: 87.86 83.74 (−4.7%)

SD: 10.08 8.07 (−20.0%)

SD: 0.89 0.70 (−21.9%)

SD: 2.61 NI (−100%)

SD: 89.42 87.44 (−2.2%)

Use of cryptic splice site in exon 3

r.[131-134del]

Class 5

c.213−1G>A

332−1G>A

Intron 5

SA: 85.51 NI (−100%)

SA: 4.84 NI (−100%)

NI NI

NI NI

SA: 89.39 NI (−100%)

Use of cryptic splice site in intron 5

r.[212_213ins213-59_213-1; 213-1g>a]

Class 5

c.302−15C>G

421-15C>G

Intron 6

SD: 91.50 91.50 (0%)

SA: 11.68 10.21 (−12.6%)

SA: 0.99 0.98 (−0.5%)

SA: 8.44 6.46 (−23.4%)

SA: 87.76 87.76 (0%)

No aberration

r.[=]

Class 2

c.547+14delG

666+14delG

Intron 8

SD: 81.89 81.89 (0%)

SD: 9.08 9.08 (0%)

SD: 0.93 0.93 (0%)

SD: 1.08 0.74 (−31.4%)

SD: 91.23 91.23 (0%)

No aberration

r.[=]

Class 2

c.670+1delG

789+1delG

Intron 10

SD: 73.32 NI (−100%)

SD: 5.98 NI (−100%)

SD: 0.89 NI (−100%)

NI NI

SD: 79.94 NI (−100%)

Use of cryptic splice site in exon 10

r.[670del]

Class 4

c.670+16G>A

789+16G>A

Intron 10

SD: 73.32 73.32 (0%)

SD: 5.98 5.98 (0%)

SD: 0.89 0.89 (0%)

NI NI

SD: 79.94 79.94 (0%)

Increased inclusion of exon 10

 

Class 3

c.4185+1G>A

4304+1G>A

Intron 12

SD: 82.52 NI (−100%)

SD: 8.59 NI (−100%)

SD: 0.95 NI (−100%)

SD: 5.17 NI (−100%)

SD: 85.50 NI (−100%)

Skipping of exon 12

r.[4097_4185del]

Class 5

c.4676−20A>G

4795−20A>G

Intron 15

SA: 84.71 84.71 (0%)

SA: 10.20 9.30 (−8.8%)

SA: 0.92 0.89 (−3.3%)

SA: 9.08 7.09 (−21.9%)

SA: 89.79 89.79 (0%)

No aberration

r.[=]

Class 2

c.4987-21G>T

5106−21G>T

Intron 16

SA: 84.55 84.55 (0%)

SA: 6.69 6.69 (0%)

SA: 0.61 0.74 (+20.9%)

SA: 1.36 1.91 (+40.6%)

SA: 87.03 87.03 (0%)

No aberration

r.[=]

Class 2

c.5075-1G>C

5194−1G>C

Intron 17

SA: 92.62 NI (−100%)

SA: 8.96 NI (−100%)

SA: 0.89 NI (−100%)

SA: 8.21 NI (−100%)

SA: 91.29 NI (−100%)

Skipping of exon 18

r.[5075_5152del]

Class 5

c.5278−14C>G

5397−14C>G

Intron 20

SA: 90.05 90.05 (0%)

SA: 13.07 12.43 (−4.9%)

SA: 0.99 0.99 (0%)

SA: 14.41 12.59 (−12.7%)

SA: 93.64 93.64 (0%)

No aberration

r.[=]

Class 2

  1. Abbreviations: NI, not identified; SA, splice acceptor; SD, splice donor; wt, wild type.
  2. The thresholds represent score predicted for wt sequence/score predicted for variant sequence. Scores indicate the values for SD or SA sites, respectively.
  3. Changes relative to wild-type sequences are indicated in % (bold if >10%).
  4. aThe 5-Tier splicing classification is based onWhiley et al.29 and Spurdle et al.30