Colon Cancer: Gene >> TRIP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000200457
Start	100868211:100868211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371631775
CDS Mutation	c.341C>T
AA Mutation	p.Ala114Val(p.A114V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000200457
Start	100870373:100870373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739C>T
AA Mutation	p.Pro247Ser(p.P247S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000200457
Start	100871654:100871654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139848707
CDS Mutation	c.1111G>A
AA Mutation	p.Gly371Ser(p.G371S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000200457
Start	100871562:100871562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019C>T
AA Mutation	p.Ala340Val(p.A340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000200457
Start	100868839:100868839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565995134
CDS Mutation	c.708A>C
AA Mutation	p.Arg236Ser(p.R236S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000200457
Start	100870637:100870637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778782117
CDS Mutation	c.893G>A
AA Mutation	p.Arg298His(p.R298H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000200457
Start	100868858:100868858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>A
AA Mutation	p.Gly243Arg(p.G243R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000200457
Start	100867945:100867945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194G>T
AA Mutation	p.Gly65Val(p.G65V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200457
Start	100870611:100870611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200457
Start	100868155:100868155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145233601
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200457
Start	100868212:100868212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200457
Start	100868861:100868861(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.733delC
AA Mutation	p.Gln245ArgfsTer4(p.Q245Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200457
Start	100868124:100868124(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.260delG
AA Mutation	p.Gly87AlafsTer11(p.G87Afs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRIP6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200457
Start	100868674:100868674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765798443
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000200457
Start	100872694:100872694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249A>T
AA Mutation	p.Arg417Ter(p.R417*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript