Colon Cancer: Gene >> EDN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379375
Start	12292497:12292497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221T>G
AA Mutation	p.Val74Gly(p.V74G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379375
Start	12293992:12293992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285G>T
AA Mutation	p.Glu95Asp(p.E95D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379375
Start	12292381:12292381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379375
Start	12294328:12294328(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.461delA
AA Mutation	p.Lys154SerfsTer7(p.K154Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000379375
Start	12294370:12294372(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs748806941
CDS Mutation	c.504_506delAAG
AA Mutation	p.Arg168del(p.R168del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EDN1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379375
Start	12294073:12294073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366T>C
Mutation Classification	Silent
Feature Type	Transcript