Colon Cancer: Gene >> IL1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263341
Start	112832754:112832754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766684369
CDS Mutation	c.374C>T
AA Mutation	p.Thr125Met(p.T125M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263341
Start	112831327:112831327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144433180
CDS Mutation	c.562G>A
AA Mutation	p.Val188Met(p.V188M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263341
Start	112836197:112836197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33G>T
AA Mutation	p.Met11Ile(p.M11I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263341
Start	112830433:112830433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738G>A
AA Mutation	p.Met246Ile(p.M246I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263341
Start	112836208:112836208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762704392
CDS Mutation	c.22G>A
AA Mutation	p.Ala8Thr(p.A8T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263341
Start	112833523:112833523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775562734
CDS Mutation	c.152G>A
AA Mutation	p.Arg51Gln(p.R51Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript