Colon Cancer: Gene >> CXCL9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264888
Start	76003635:76003635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139830877
CDS Mutation	c.341G>A
AA Mutation	p.Arg114Gln(p.R114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264888
Start	76003623:76003623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764068063
CDS Mutation	c.353G>A
AA Mutation	p.Arg118His(p.R118H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264888
Start	76003653:76003653(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.323delA
AA Mutation	p.Lys108ArgfsTer4(p.K108Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264888
Start	76004808:76004808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747595704
CDS Mutation	c.276+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CXCL9

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000264888
Start	76003636:76003636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757038649
CDS Mutation	c.340C>T
AA Mutation	p.Arg114Ter(p.R114*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript