Colon Cancer: Gene >> BRIX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336767
Start	34922748:34922748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201632829
CDS Mutation	c.490C>T
AA Mutation	p.Pro164Ser(p.P164S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336767
Start	34924900:34924900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000336767
Start	34923037:34923037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.547G>T
AA Mutation	p.Glu183Ter(p.E183*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BRIX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336767
Start	34915800:34915800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62G>T
AA Mutation	p.Arg21Ile(p.R21I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336767
Start	34924890:34924890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707T>G
AA Mutation	p.Phe236Cys(p.F236C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336767
Start	34919880:34919880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370425530
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript