Colon Cancer: Gene >> ELOVL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369816
Start	79924969:79924969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352A>G
AA Mutation	p.Asn118Asp(p.N118D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369816
Start	79916793:79916793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760T>A
AA Mutation	p.Tyr254Asn(p.Y254N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369816
Start	79926376:79926376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106C>T
AA Mutation	p.Arg36Cys(p.R36C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369816
Start	79925010:79925010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200915130
CDS Mutation	c.311C>T
AA Mutation	p.Ala104Val(p.A104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000369816
Start	79916616:79916616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937G>T
AA Mutation	p.Gly313Ter(p.G313*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ELOVL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369816
Start	79919455:79919455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634C>A
AA Mutation	p.Leu212Ile(p.L212I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript