Colon Cancer: Gene >> FKTN

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000223528
Start	105635053:105635053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1175A>G
AA Mutation	p.Tyr392Cys(p.Y392C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223528
Start	105575108:105575108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.76T>C
AA Mutation	p.Tyr26His(p.Y26H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223528
Start	105596620:105596620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128C>G
AA Mutation	p.Ser43Cys(p.S43C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223528
Start	105635063:105635063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141886790
CDS Mutation	c.1185G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000223528
Start	105619989:105619989(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs750176716
CDS Mutation	c.1106delT
AA Mutation	p.Phe369SerfsTer37(p.F369Sfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000223528
Start	105607937:105607937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377417974
CDS Mutation	c.766C>T
AA Mutation	p.Arg256Ter(p.R256*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FKTN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223528
Start	105601161:105601161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.182T>G
AA Mutation	p.Phe61Cys(p.F61C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223528
Start	105635114:105635114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript