Colon Cancer: Gene >> CXCR6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304552
Start	45946570:45946570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89G>A
AA Mutation	p.Ser30Asn(p.S30N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304552
Start	45946577:45946577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.96C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304552
Start	45947291:45947291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304552
Start	45946826:45946826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576262442
CDS Mutation	c.345G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CXCR6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304552
Start	45946594:45946594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113A>C
AA Mutation	p.Tyr38Ser(p.Y38S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304552
Start	45946523:45946523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42T>C
Mutation Classification	Silent
Feature Type	Transcript