Colon Cancer: Gene >> UCHL1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000284440
Start	41261921:41261921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139583787
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Trp(p.R153W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284440
Start	41261899:41261899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142811772
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284440
Start	41264122:41264122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> UCHL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284440
Start	41263231:41263231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466G>T
AA Mutation	p.Asp156Tyr(p.D156Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284440
Start	41268050:41268050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770039881
CDS Mutation	c.649G>A
AA Mutation	p.Val217Met(p.V217M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript