Colon Cancer: Gene >> TFPI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222543
Start	93889100:93889100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113538343
CDS Mutation	c.395G>A
AA Mutation	p.Arg132Gln(p.R132Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222543
Start	93886863:93886863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543669576
CDS Mutation	c.665G>A
AA Mutation	p.Arg222His(p.R222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222543
Start	93890650:93890650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29C>T
AA Mutation	p.Ser10Leu(p.S10L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222543
Start	93887421:93887421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471T>G
AA Mutation	p.Phe157Leu(p.F157L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222543
Start	93890212:93890212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196T>C
AA Mutation	p.Tyr66His(p.Y66H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222543
Start	93890173:93890173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235T>C
AA Mutation	p.Trp79Arg(p.W79R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222543
Start	93890192:93890192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TFPI2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222543
Start	93890238:93890238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.170A>G
AA Mutation	p.Tyr57Cys(p.Y57C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript