Colon Cancer: Gene >> UGCG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374279
Start	111931300:111931300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767T>C
AA Mutation	p.Val256Ala(p.V256A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374279
Start	111897294:111897294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79T>G
AA Mutation	p.Phe27Val(p.F27V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374279
Start	111914732:111914732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.226T>A
AA Mutation	p.Leu76Met(p.L76M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374279
Start	111922876:111922876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268C>A
AA Mutation	p.His90Asn(p.H90N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374279
Start	111932269:111932269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374279
Start	111932900:111932900(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1094delT
AA Mutation	p.Leu365CysfsTer9(p.L365Cfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> UGCG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374279
Start	111931333:111931333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800C>A
AA Mutation	p.Ser267Tyr(p.S267Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374279
Start	111929535:111929535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594C>A
Mutation Classification	Silent
Feature Type	Transcript