Colon Cancer: Gene >> TRIB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217233
Start	391411:391411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199753662
CDS Mutation	c.416G>A
AA Mutation	p.Arg139Gln(p.R139Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217233
Start	396266:396266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.653A>G
AA Mutation	p.Asp218Gly(p.D218G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217233
Start	396447:396447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375469008
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217233
Start	391499:391499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217233
Start	388208:388208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217233
Start	396288:396288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564546115
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000217233
Start	388140:388140(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs745734359
CDS Mutation	c.135delC
AA Mutation	p.Cys46AlafsTer5(p.C46Afs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRIB3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217233
Start	396441:396441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746757202
CDS Mutation	c.828G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000217233
Start	388116:388116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150841542
CDS Mutation	c.106C>T
AA Mutation	p.Arg36Ter(p.R36*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript