Colon Cancer: Gene >> IL26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229134
Start	68225164:68225164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348G>T
AA Mutation	p.Gln116His(p.Q116H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229134
Start	68202031:68202031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.416G>T
AA Mutation	p.Arg139Ile(p.R139I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229134
Start	68225196:68225196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373868127
CDS Mutation	c.316C>T
AA Mutation	p.Arg106Cys(p.R106C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229134
Start	68201859:68201859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502G>A
AA Mutation	p.Glu168Lys(p.E168K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229134
Start	68225238:68225238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>T
AA Mutation	p.Asp92Tyr(p.D92Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000229134
Start	68225478:68225478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371094808
CDS Mutation	c.194G>A
AA Mutation	p.Arg65Gln(p.R65Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000229134
Start	68225486:68225486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186A>C
AA Mutation	p.Lys62Asn(p.K62N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229134
Start	68225633:68225633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124G>T
AA Mutation	p.Val42Phe(p.V42F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript