Colon Cancer: Gene >> IFNG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229135
Start	68159511:68159511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105G>T
AA Mutation	p.Lys35Asn(p.K35N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229135
Start	68158023:68158023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.256G>T
AA Mutation	p.Asp86Tyr(p.D86Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000229135
Start	68157914:68157914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365C>T
AA Mutation	p.Ser122Leu(p.S122L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229135
Start	68158057:68158057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229135
Start	68157934:68157934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572179856
CDS Mutation	c.345C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IFNG

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229135
Start	68157934:68157934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572179856
CDS Mutation	c.345C>T
Mutation Classification	Silent
Feature Type	Transcript