Colon Cancer: Gene >> CXCL16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293778
Start	4738872:4738872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756648834
CDS Mutation	c.185G>T
AA Mutation	p.Arg62Ile(p.R62I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293778
Start	4738843:4738843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214C>A
AA Mutation	p.Gln72Lys(p.Q72K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293778
Start	4735105:4735105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138114709
CDS Mutation	c.762G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293778
Start	4739334:4739334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538625577
CDS Mutation	c.63A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293778
Start	4735422:4735422(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.445delG
AA Mutation	p.Ala149HisfsTer26(p.A149Hfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293778
Start	4738842:4738843(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.214_215insG
AA Mutation	p.Gln72ArgfsTer46(p.Q72Rfs*46)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000293778
Start	4735510:4735510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CXCL16

No Mutation Annotation!