Colon Cancer: Gene >> CXCR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373693
Start	71616619:71616619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853G>A
AA Mutation	p.Ala285Thr(p.A285T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373693
Start	71616972:71616972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500G>A
AA Mutation	p.Arg167His(p.R167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373693
Start	71616998:71616998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.474G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373693
Start	71617343:71617343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373693
Start	71616971:71616971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373693
Start	71617007:71617007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.465T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373693
Start	71616527:71616527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373693
Start	71617307:71617307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373693
Start	71616978:71616978(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.494delC
AA Mutation	p.Pro165ArgfsTer4(p.P165Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CXCR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373693
Start	71616886:71616886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586G>A
AA Mutation	p.Glu196Lys(p.E196K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373693
Start	71616527:71616527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript