Colon Cancer: Gene >> CFP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247153
Start	47627623:47627623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Gly141Asp(p.G141D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247153
Start	47627159:47627159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs8177077
CDS Mutation	c.748G>A
AA Mutation	p.Gly250Ser(p.G250S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247153
Start	47629595:47629595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247153
Start	47628217:47628217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247153
Start	47628229:47628229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749722640
CDS Mutation	c.276G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247153
Start	47626493:47626493(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.967delG
AA Mutation	p.Glu323SerfsTer10(p.E323Sfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000247153
Start	47629817:47629817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28C>T
AA Mutation	p.Arg10Ter(p.R10*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247153
Start	47624368:47624369(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1316_1317insGCTAGTTTAT
AA Mutation	p.Cys439TrpfsTer5(p.C439Wfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CFP

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247153
Start	47627160:47627160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000247153
Start	47626385:47626385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075C>T
AA Mutation	p.Arg359Ter(p.R359*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript