Colon Cancer: Gene >> TRIM21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254436
Start	4390235:4390235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175C>A
AA Mutation	p.Leu59Met(p.L59M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254436
Start	4385337:4385337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1376C>A
AA Mutation	p.Pro459His(p.P459H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254436
Start	4385541:4385541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172G>A
AA Mutation	p.Gly391Asp(p.G391D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254436
Start	4385603:4385603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254436
Start	4390341:4390341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779542271
CDS Mutation	c.69C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254436
Start	4385685:4385685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028A>G
AA Mutation	p.Tyr343Cys(p.Y343C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000254436
Start	4390178:4390178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232G>T
AA Mutation	p.Glu78Ter(p.E78*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript