Colon Cancer: Gene >> UGT1A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373414
Start	233713686:233713686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779646185
CDS Mutation	c.695C>T
AA Mutation	p.Ala232Val(p.A232V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373414
Start	233713520:233713520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529C>T
AA Mutation	p.Pro177Ser(p.P177S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373414
Start	233713207:233713207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757096232
CDS Mutation	c.216G>T
AA Mutation	p.Glu72Asp(p.E72D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373414
Start	233713489:233713489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17868332
CDS Mutation	c.498G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000373414
Start	233713001:233713001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10G>T
AA Mutation	p.Gly4Ter(p.G4*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UGT1A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373414
Start	233713767:233713767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776G>A
AA Mutation	p.Gly259Glu(p.G259E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000373414
Start	233713202:233713202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181492639
CDS Mutation	c.211G>T
AA Mutation	p.Glu71Ter(p.E71*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript