Colon Cancer: Gene >> IGFBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275521
Start	45916552:45916552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746A>T
AA Mutation	p.Lys249Met(p.K249M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275521
Start	45916615:45916615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683A>G
AA Mutation	p.Asn228Ser(p.N228S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000275521
Start	45914944:45914944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.752G>A
AA Mutation	p.Cys251Tyr(p.C251Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000275521
Start	45917243:45917243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>A
AA Mutation	p.Phe200Leu(p.F200L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000275521
Start	45917224:45917224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768974204
CDS Mutation	c.619G>C
AA Mutation	p.Glu207Gln(p.E207Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275521
Start	45917372:45917372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000275521
Start	45917341:45917341(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.502delC
AA Mutation	p.Leu168SerfsTer5(p.L168Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IGFBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275521
Start	45916558:45916558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740A>C
AA Mutation	p.Lys247Thr(p.K247T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275521
Start	45917273:45917273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766767739
CDS Mutation	c.570C>T
Mutation Classification	Silent
Feature Type	Transcript