Colon Cancer: Gene >> TRIM59

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309784
Start	160438424:160438424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.760G>C
AA Mutation	p.Val254Leu(p.V254L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309784
Start	160438830:160438830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309784
Start	160438371:160438371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769978259
CDS Mutation	c.813G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM59

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309784
Start	160438535:160438535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649G>A
AA Mutation	p.Glu217Lys(p.E217K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309784
Start	160438152:160438152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753946979
CDS Mutation	c.1032G>A
Mutation Classification	Silent
Feature Type	Transcript