Colon Cancer: Gene >> FGF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228837
Start	4445383:4445383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17183529
CDS Mutation	c.188C>T
AA Mutation	p.Ala63Val(p.A63V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228837
Start	4445384:4445384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148657794
CDS Mutation	c.187G>A
AA Mutation	p.Ala63Thr(p.A63T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228837
Start	4434280:4434280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142642694
CDS Mutation	c.562C>T
AA Mutation	p.Arg188Trp(p.R188W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228837
Start	4445556:4445556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228837
Start	4445385:4445385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202212518
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228837
Start	4445496:4445496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17183515
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000228837
Start	4444210:4444210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779702937
CDS Mutation	c.373C>T
AA Mutation	p.Arg125Ter(p.R125*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FGF6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228837
Start	4444169:4444169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767833262
CDS Mutation	c.414C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228837
Start	4445385:4445385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202212518
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript