Colon Cancer: Gene >> IGFBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233809
Start	216661982:216661982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797T>C
AA Mutation	p.Leu266Pro(p.L266P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233809
Start	216663997:216663997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871G>A
AA Mutation	p.Gly291Arg(p.G291R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233809
Start	216661936:216661936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751G>A
AA Mutation	p.Glu251Lys(p.E251K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233809
Start	216660627:216660627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776916285
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233809
Start	216660628:216660628(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.518delG
AA Mutation	p.Gly173GlufsTer13(p.G173Efs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IGFBP2

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000233809
Start	216660769:216660769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Ter(p.R219*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript