Colon Cancer: Gene >> BCL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333681
Start	63318662:63318662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5C>T
AA Mutation	p.Ala2Val(p.A2V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333681
Start	63128726:63128726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748122615
CDS Mutation	c.619C>T
AA Mutation	p.Arg207Trp(p.R207W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333681
Start	63318313:63318313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333681
Start	63318301:63318301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BCL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333681
Start	63318585:63318585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82T>C
AA Mutation	p.Tyr28His(p.Y28H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript