Colon Cancer: Gene >> CCR8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326306
Start	39333157:39333157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826C>A
AA Mutation	p.Gln276Lys(p.Q276K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326306
Start	39333325:39333325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.994A>G
AA Mutation	p.Arg332Gly(p.R332G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326306
Start	39332695:39332695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364T>C
AA Mutation	p.Phe122Leu(p.F122L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326306
Start	39332451:39332451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326306
Start	39332964:39332964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326306
Start	39333381:39333381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140234572
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326306
Start	39333077:39333077(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.749delT
AA Mutation	p.Phe250SerfsTer25(p.F250Sfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CCR8

No Mutation Annotation!