Colon Cancer: Gene >> IGFBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275525
Start	45890695:45890695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497T>C
AA Mutation	p.Val166Ala(p.V166A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275525
Start	45891942:45891942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369196046
CDS Mutation	c.530G>A
AA Mutation	p.Arg177Gln(p.R177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275525
Start	45892046:45892046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747950009
CDS Mutation	c.634T>C
AA Mutation	p.Tyr212His(p.Y212H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000275525
Start	45892979:45892979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668G>T
AA Mutation	p.Gly223Val(p.G223V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000275525
Start	45893085:45893085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774A>C
AA Mutation	p.Gln258His(p.Q258H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IGFBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275525
Start	45890658:45890658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566229997
CDS Mutation	c.460G>A
AA Mutation	p.Ala154Thr(p.A154T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript