Colon Cancer: Gene >> TFPI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233156
Start	187467855:187467855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.706A>G
AA Mutation	p.Asn236Asp(p.N236D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233156
Start	187467030:187467030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821G>T
AA Mutation	p.Arg274Ile(p.R274I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233156
Start	187497027:187497027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568113767
CDS Mutation	c.173C>T
AA Mutation	p.Ala58Val(p.A58V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233156
Start	187467831:187467831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730C>A
AA Mutation	p.Pro244Thr(p.P244T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233156
Start	187496962:187496962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238G>A
AA Mutation	p.Glu80Lys(p.E80K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233156
Start	187496963:187496963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145282588
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233156
Start	187497026:187497026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780564015
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000233156
Start	187484917:187484917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429T>G
AA Mutation	p.Tyr143Ter(p.Y143*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233156
Start	187467805:187467806(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.755dupG
AA Mutation	p.Asn253LysfsTer2(p.N253Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TFPI

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233156
Start	187503757:187503757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000233156
Start	187466959:187466959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.892G>T
AA Mutation	p.Glu298Ter(p.E298*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000233156
Start	187503666:187503666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103G>T
AA Mutation	p.Glu35Ter(p.E35*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript