Colon Cancer: Gene >> IL10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000423557
Start	206770912:206770912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.373C>T
AA Mutation	p.Arg125Cys(p.R125C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000423557
Start	206770948:206770948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Gly113Arg(p.G113R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423557
Start	206770964:206770964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560908141
CDS Mutation	c.321G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IL10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000423557
Start	206768643:206768643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376415487
CDS Mutation	c.530G>A
AA Mutation	p.Arg177Gln(p.R177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000423557
Start	206769885:206769885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388C>A
AA Mutation	p.Leu130Ile(p.L130I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000423557
Start	206770943:206770943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.342G>T
AA Mutation	p.Glu114Asp(p.E114D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript