Colon Cancer: Gene >> CNR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374472
Start	23874608:23874608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010T>C
AA Mutation	p.Val337Ala(p.V337A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374472
Start	23875004:23875004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614T>C
AA Mutation	p.Ile205Thr(p.I205T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374472
Start	23875174:23875174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.444A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CNR2

No Mutation Annotation!