Colon Cancer: Gene >> CEACAM8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244336
Start	42589026:42589026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716C>T
AA Mutation	p.Ala239Val(p.A239V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244336
Start	42588886:42588886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856A>G
AA Mutation	p.Ile286Val(p.I286V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244336
Start	42593694:42593694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.271C>G
AA Mutation	p.Pro91Ala(p.P91A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244336
Start	42589602:42589602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554918701
CDS Mutation	c.558G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244336
Start	42588860:42588860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185392969
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CEACAM8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244336
Start	42589607:42589607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553C>A
AA Mutation	p.Leu185Ile(p.L185I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244336
Start	42593636:42593636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45440298
CDS Mutation	c.329G>A
AA Mutation	p.Arg110Gln(p.R110Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244336
Start	42593875:42593875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369527473
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript