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Table 1 TF mutation status in cancers from the Cbioportal database (www.cbioportal.org)

From: Tissue factor (coagulation factor III): a potential double-edge molecule to be targeted and re-targeted toward cancer

Cancer type

Protein change

Mutation

Mutation type

COSMIC sample ID

Head and Neck Squamous Cell Carcinoma

F3-C11ORF80

-

Fusion

TCGA-D6-6517–01

F3-C11ORF80

-

Fusion

TCGA-F7-A620-01

I70V

1:g.95005817 T > C

Missense

TCGA-UF-A71A-01

X251_splice

1:g.94997876C > T

Splice_Site

TCGA-CR-7399–01

Serous Ovarian Cancer

P238R

1:g.94997915G > C

Missense

TCGA-23–2649-01

K233N

1:g.94997929C > A

Missense

TCGA-04–1648-01

Glioblastoma Multiforme

X71_splice

1:g.95001720G > A

Splice_Region

TCGA-12–0775-01

D93N

1:g.95001656C > T

Missense

TCGA-19–5956-01

Lung Squamous Cell Carcinoma

S174R

1:g.94998715G > C

Missense

TCGA-85–6560-01

Y189C

1:g.94998671 T > C

Missense

TCGA-56–8504-01

Bladder Urothelial Carcinoma

L274V

1:g.94996084G > C

Missense

TCGA-XF-A8HE-01

Uterine Endometrioid Carcinoma

G141R

1:g.94998816C > T

Missense

TCGA-AX-A2HD-01

C81F

1:g.95001691C > A

Missense

TCGA-AP-A0LM-01

K181N

1:g.94998694C > A

Missense

TCGA-D1-A17Q-01

E127D

1:g.95001552C > A

Missense

TCGA-D1-A17Q-01

Q222H

1:g.94997962 T > G

Missense

TCGA-BS-A0UV-01

L44*

1:g.95005894A > C

Nonsense

TCGA-AX-A05Z-01

T87Rfs*3

1:g.95001672_95001673del

Frame_Shift_Del

TCGA-AX-A3FS-01

N170T

1:g.94998728 T > G

Missense

TCGA-B5-A3FC-01

A112T

1:g.95001599C > T

Missense

TCGA-B5-A3FC-01

E215*

1:g.94997985C > A

Nonsense

TCGA-E6-A1LX-01

X251_splice

1:g.94996151 T > C

Splice_Region

TCGA-EO-A22R-01

Lung Adenocarcinoma

L55*

1:g.95005860_95005861del

Frame_Shift_Del

TCGA-05–4396-01

N114Y

1:g.95001593 T > A

Missense

TCGA-97-A4LX-01

Cutaneous Melanoma

N231T

1:g.94997936 T > G

Missense

TCGA-EB-A24D-01

E2K

1:g.95007189C > T

Missense

TCGA-GN-A26C-01

V260I

1:g.94996126C > T

Missense

TCGA-D9-A6EA-06

E94G

1:g.95001652 T > C

Missense

TCGA-D9-A6EC-06

R168K

1:g.94998734C > T

Missense

TCGA-D3-A8GM-06

S129F

1:g.95001547G > A

Missense

TCGA-FR-A8YE-06

Diffuse Type Stomach Adenocarcinoma

F179Lfs*5

1:g.94998700del

Frame_Shift_Del

TCGA-CG-4465–01

Tubular Stomach Adenocarcinoma

A200T

1:g.94998030C > T

Missense

TCGA-HU-A4GQ-01

L175I

1:g.94998714G > T

Missense

TCGA-ZQ-A9CR-01

Colon Adenocarcinoma

S174N

1:g.94998716C > T

Missense

TCGA-AA-3858–01

Y135C

1:g.95001529 T > C

Missense

TCGA-5 M-AAT6-01

Rectal Adenocarcinoma

N43D

1:g.95005898 T > C

Missense

TCGA-AG-A002-01

D177Y

1:g.94998708C > A

Missense

TCGA-EI-6513–01

  1. Its (*) part of mutation's name. The asterisk (*) is often used to denote a specific type of mutation called a stop codon mutation or a nonsense mutation. A stop codon is a specific sequence of DNA that signals the end of a protein-coding region. When a mutation occurs at this stop codon, it can result in a premature termination of protein synthesis