Colon Cancer: Gene >> CTSV

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259470
Start	97037580:97037580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162G>T
AA Mutation	p.Lys54Asn(p.K54N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259470
Start	97037556:97037556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259470
Start	97035613:97035613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.702G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259470
Start	97038032:97038032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000259470
Start	97035694:97035694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.622-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CTSV

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259470
Start	97035667:97035667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.648G>T
AA Mutation	p.Glu216Asp(p.E216D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259470
Start	97036657:97036657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757644240
CDS Mutation	c.487G>A
AA Mutation	p.Glu163Lys(p.E163K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript