Colon Cancer: Gene >> SLC15A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266771
Start	128814932:128814932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685C>T
AA Mutation	p.Pro229Ser(p.P229S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266771
Start	128814937:128814937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376967004
CDS Mutation	c.680C>T
AA Mutation	p.Ala227Val(p.A227V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266771
Start	128794236:128794236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372794236
CDS Mutation	c.1694G>A
AA Mutation	p.Arg565Gln(p.R565Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266771
Start	128794204:128794204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1726A>G
AA Mutation	p.Arg576Gly(p.R576G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266771
Start	128799287:128799287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143396970
CDS Mutation	c.1545C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC15A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266771
Start	128814911:128814911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706G>A
AA Mutation	p.Ala236Thr(p.A236T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266771
Start	128810055:128810055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899A>G
AA Mutation	p.Lys300Arg(p.K300R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript