Colon Cancer: Gene >> TREM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244709
Start	41282511:41282511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113487579
CDS Mutation	c.290G>A
AA Mutation	p.Arg97His(p.R97H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244709
Start	41282412:41282412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780834156
CDS Mutation	c.389G>A
AA Mutation	p.Arg130His(p.R130H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244709
Start	41282536:41282536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265G>A
AA Mutation	p.Asp89Asn(p.D89N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000244709
Start	41280967:41280967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593T>C
AA Mutation	p.Ile198Thr(p.I198T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000244709
Start	41282418:41282418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>A
AA Mutation	p.Arg128His(p.R128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244709
Start	41281062:41281062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244709
Start	41276209:41276209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000244709
Start	41282752:41282752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TREM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244709
Start	41282733:41282733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68A>C
AA Mutation	p.Lys23Thr(p.K23T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript