Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IGBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342206
Start	70134107:70134107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160G>A
AA Mutation	p.Glu54Lys(p.E54K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342206
Start	70134645:70134645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311G>A
AA Mutation	p.Arg104Gln(p.R104Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342206
Start	70148817:70148817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342206
Start	70134577:70134577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IGBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342206
Start	70146718:70146718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568C>T
AA Mutation	p.Arg190Cys(p.R190C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342206
Start	70146785:70146785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635A>G
AA Mutation	p.Asp212Gly(p.D212G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342206
Start	70133975:70133975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28C>T
AA Mutation	p.Pro10Ser(p.P10S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000342206
Start	70165964:70165964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003C>T
AA Mutation	p.Arg335Ter(p.R335*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript