Colon Cancer: Gene >> TEF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266304
Start	41387361:41387361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168G>T
AA Mutation	p.Lys56Asn(p.K56N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000406644
Start	41367554:41367554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22A>G
AA Mutation	p.Lys8Glu(p.K8E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266304
Start	41395793:41395793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Trp(p.R249W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266304
Start	41387431:41387431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238C>T
AA Mutation	p.Pro80Ser(p.P80S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266304
Start	41395878:41395878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367638171
CDS Mutation	c.830C>T
AA Mutation	p.Thr277Met(p.T277M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TEF

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266304
Start	41387466:41387466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762802821
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266304
Start	41394295:41394295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675C>A
Mutation Classification	Silent
Feature Type	Transcript