Colon Cancer: Gene >> TFF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000291526
Start	42347599:42347599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263G>C
AA Mutation	p.Arg88Pro(p.R88P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000291526
Start	42350942:42350942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142559683
CDS Mutation	c.16G>A
AA Mutation	p.Ala6Thr(p.A6T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000291526
Start	42350896:42350896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139956370
CDS Mutation	c.62C>T
AA Mutation	p.Ala21Val(p.A21V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291526
Start	42350005:42350005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291526
Start	42347499:42347499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TFF2

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000291526
Start	42350948:42350948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10C>T
AA Mutation	p.Arg4Ter(p.R4*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript