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Table 3 10 optimal feature genes contained in the SVM classifier

From: A risk model of gene signatures for predicting platinum response and survival in ovarian cancer

Gene

DE mRNA

DE CN

Variant

logFC

p.value

logFC

p.value

Chrom

Variant Position

Type

Variant Classification

Amino acids

Codons

Reference Allele

Tumor Allele

dbSNP_RS

CD209

0.358543

0.0142

−0.42485

0.012717

19

7,807,996

SNP

Missense

R

Agg/Cgg

C

T

rs11465393

CD274

0.437529

0.00976

0.460916

0.002227

9

5,462,907

SNP

Missense

G/V

gGg/gTg

G

T

novel

HIST1H3I

−0.43754

0.00255

0.30903

0.010138

6

27,839,796

SNP

Missense

P/LX

cca/cTca

A

G

novel

HIST1H4L

−0.43335

0.0143

0.30903

0.010138

6

27,841,216

SNP

Missense

T

acA/acG

C

T

novel

NLGN1

1.019701

0.00143

0.351201

0.004621

3

173,525,589

SNP

Missense

T/M

aCg/aTg

G

C

novel

NTRK3

−0.36699

0.0247

0.295746

0.007258

15

88,576,170

SNP

Silent

L

Ctg/Ttg

C

G

novel

88,483,904

SNP

Nonsense

T

acG/acC

C

A

novel

88,522,597

SNP

Intron

R/W

Cgg/Tgg

G

A

novel

88,423,602

SNP

Missense

T

acG/acA

G

A

novel

88,420,205

SNP

Missense

D/X

Gat/at

C

A

novel

88,476,380

SNP

Missense

Y

taC/taT

A

T

novel

PNLDC1

−0.85134

0.000718

−0.34754

0.003742

6

160,240,313

SNP

Silent

I/M

atC/atG

G

C

novel

SLC22A3

−0.51215

0.0225

−0.30286

0.005976

6

160,872,083

SNP

Missense

Y/*

taC/taG

C

T

novel

SLC5A1

0.298462

0.00642

0.441319

0.001623

22

32,495,226

SNP

Nonsense

V

gtC/gtT

C

G

novel

SYNM

0.558712

0.00288

0.448385

0.001034

15

99,672,483

SNP

Silent

T/R

aCg/aGg

A

G

novel

99,669,768

SNP

Silent

T

acC/acT

G

A

novel

99,671,917

SNP

Missense

R

cgG/cgC

G

C

novel

99,672,905

SNP

Missense

T/N

aCc/aAc

C

G

novel

99,653,864

SNP

Silent

D/E

gaT/gaA

C

T

novel

99,672,085

SNP

Missense

Y/H

Tac/Cac

G

T

novel