Colon Cancer: Gene >> IL27

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356897
Start	28503986:28503986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.96C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356897
Start	28502129:28502129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356897
Start	28499807:28499807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570953144
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356897
Start	28502023:28502023(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.415delG
AA Mutation	p.Ala139ProfsTer2(p.A139Pfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000356897
Start	28506780:28506780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.31+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IL27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356897
Start	28504005:28504005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77T>C
AA Mutation	p.Val26Ala(p.V26A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript