Colon Cancer: Gene >> NODAL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287139
Start	70435975:70435975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202G>A
AA Mutation	p.Val68Met(p.V68M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287139
Start	70435770:70435770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407T>G
AA Mutation	p.Leu136Arg(p.L136R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287139
Start	70441518:70441518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287139
Start	70433020:70433020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.960G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NODAL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287139
Start	70435359:70435359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818C>T
AA Mutation	p.Ala273Val(p.A273V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript