Colon Cancer: Gene >> TTL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233336
Start	112485976:112485976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217C>T
AA Mutation	p.Arg73Cys(p.R73C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233336
Start	112494290:112494290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384A>C
AA Mutation	p.Arg128Ser(p.R128S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233336
Start	112494302:112494302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754448506
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000233336
Start	112494291:112494291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385G>T
AA Mutation	p.Glu129Ter(p.E129*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TTL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233336
Start	112503062:112503062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756C>A
AA Mutation	p.Asn252Lys(p.N252K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233336
Start	112494320:112494320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>T
AA Mutation	p.Lys138Asn(p.K138N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233336
Start	112502967:112502967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661C>A
AA Mutation	p.Leu221Ile(p.L221I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript