Colon Cancer: Gene >> CX3CL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000006053
Start	57383027:57383027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773596059
CDS Mutation	c.1189G>A
AA Mutation	p.Val397Met(p.V397M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000006053
Start	57382662:57382662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824T>A
AA Mutation	p.Phe275Tyr(p.F275Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000006053
Start	57382505:57382505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667G>A
AA Mutation	p.Asp223Asn(p.D223N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000006053
Start	57382992:57382992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199662906
CDS Mutation	c.1154G>A
AA Mutation	p.Arg385Gln(p.R385Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000006053
Start	57382200:57382200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362T>C
AA Mutation	p.Met121Thr(p.M121T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000006053
Start	57382354:57382354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000006053
Start	57382090:57382090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150847141
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CX3CL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000006053
Start	57382530:57382530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529786529
CDS Mutation	c.692C>T
AA Mutation	p.Ala231Val(p.A231V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript