Colon Cancer: Gene >> TOM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000449058
Start	35327311:35327311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.689A>G
AA Mutation	p.Asn230Ser(p.N230S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000449058
Start	35330363:35330363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782G>A
AA Mutation	p.Cys261Tyr(p.C261Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449058
Start	35333418:35333418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000449058
Start	35333424:35333424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141753674
CDS Mutation	c.954G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000449058
Start	35323625:35323625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496C>T
AA Mutation	p.Gln166Ter(p.Q166*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TOM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000449058
Start	35323584:35323584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.455C>G
AA Mutation	p.Pro152Arg(p.P152R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript