Colon Cancer: Gene >> CX3CR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399220
Start	39266431:39266431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200139865
CDS Mutation	c.79G>A
AA Mutation	p.Val27Met(p.V27M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399220
Start	39265950:39265950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.560G>C
AA Mutation	p.Trp187Ser(p.W187S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399220
Start	39265978:39265978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532G>A
AA Mutation	p.Asp178Asn(p.D178N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399220
Start	39266107:39266107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748219184
CDS Mutation	c.403G>A
AA Mutation	p.Ala135Thr(p.A135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399220
Start	39265689:39265689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821C>T
AA Mutation	p.Ala274Val(p.A274V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399220
Start	39265746:39265746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375338951
CDS Mutation	c.764C>T
AA Mutation	p.Thr255Met(p.T255M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399220
Start	39265796:39265796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399220
Start	39265916:39265916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369705104
CDS Mutation	c.594T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399220
Start	39266060:39266060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399220
Start	39265583:39265583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000399220
Start	39266482:39266482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.28G>T
AA Mutation	p.Glu10Ter(p.E10*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000399220
Start	39265957:39265957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>T
AA Mutation	p.Glu185Ter(p.E185*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399220
Start	39266088:39266089(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.421_422insTGGA
AA Mutation	p.Arg141LeufsTer35(p.R141Lfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CX3CR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399220
Start	39266198:39266198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.312C>A
AA Mutation	p.Phe104Leu(p.F104L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript