Colon Cancer: Gene >> BID

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399774
Start	17750109:17750109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8G>A
AA Mutation	p.Cys3Tyr(p.C3Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399774
Start	17738104:17738104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000399774
Start	17750175:17750175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.-58-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> BID

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399774
Start	17743899:17743899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747016844
CDS Mutation	c.127G>A
AA Mutation	p.Glu43Lys(p.E43K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399774
Start	17738083:17738083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510C>A
Mutation Classification	Silent
Feature Type	Transcript