Colon Cancer: Gene >> BLVRB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263368
Start	40458521:40458521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104G>T
AA Mutation	p.Arg35Leu(p.R35L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263368
Start	40447911:40447911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599A>G
AA Mutation	p.Tyr200Cys(p.Y200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263368
Start	40451485:40451485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263368
Start	40447928:40447928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BLVRB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263368
Start	40447947:40447947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563G>C
AA Mutation	p.Cys188Ser(p.C188S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263368
Start	40458412:40458412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213C>T
Mutation Classification	Silent
Feature Type	Transcript