Colon Cancer: Gene >> BCL2L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250405
Start	23308912:23308912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529G>C
AA Mutation	p.Ala177Pro(p.A177P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250405
Start	23308888:23308888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505T>C
AA Mutation	p.Ser169Pro(p.S169P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250405
Start	23308939:23308939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556G>A
AA Mutation	p.Val186Ile(p.V186I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250405
Start	23307896:23307896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BCL2L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250405
Start	23308017:23308017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745978918
CDS Mutation	c.250G>A
AA Mutation	p.Asp84Asn(p.D84N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript