Colon Cancer: Gene >> ENDOG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372642
Start	128822470:128822470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754G>A
AA Mutation	p.Ala252Thr(p.A252T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372642
Start	128822573:128822573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857C>T
AA Mutation	p.Ala286Val(p.A286V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372642
Start	128820826:128820826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.589A>G
AA Mutation	p.Thr197Ala(p.T197A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372642
Start	128820788:128820788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145739062
CDS Mutation	c.551G>A
AA Mutation	p.Arg184His(p.R184H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372642
Start	128822570:128822570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854G>T
AA Mutation	p.Arg285Leu(p.R285L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372642
Start	128822589:128822589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ENDOG

No Mutation Annotation!