Colon Cancer: Gene >> JUN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371222
Start	58782436:58782436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.635C>T
AA Mutation	p.Pro212Leu(p.P212L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371222
Start	58782301:58782302(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.769dupA
AA Mutation	p.Arg257LysfsTer53(p.R257Kfs*53)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371222
Start	58782872:58782873(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.198_199insT
AA Mutation	p.Gly67TrpfsTer40(p.G67Wfs*40)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> JUN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371222
Start	58782283:58782283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788G>A
AA Mutation	p.Arg263His(p.R263H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371222
Start	58782879:58782879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript