Colon Cancer: Gene >> EN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295206
Start	118843053:118843053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064G>A
AA Mutation	p.Arg355His(p.R355H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295206
Start	118846752:118846752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416G>A
AA Mutation	p.Gly139Glu(p.G139E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295206
Start	118843245:118843245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872C>T
AA Mutation	p.Thr291Ile(p.T291I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295206
Start	118843054:118843054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1063C>T
AA Mutation	p.Arg355Cys(p.R355C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295206
Start	118843181:118843181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295206
Start	118846851:118846851(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.317delT
AA Mutation	p.Phe106SerfsTer6(p.F106Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295206
Start	118846812:118846813(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.355_356insC
AA Mutation	p.Lys119ThrfsTer27(p.K119Tfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295206
Start	118846824:118846824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344T>G
AA Mutation	p.Phe115Cys(p.F115C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript