Colon Cancer: Gene >> PSMB9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374859
Start	32858407:32858407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434C>T
AA Mutation	p.Ala145Val(p.A145V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374859
Start	32858059:32858059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315T>G
AA Mutation	p.Asn105Lys(p.N105K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374859
Start	32859502:32859502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000374859
Start	32858075:32858075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Ter(p.R111*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PSMB9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374859
Start	32857309:32857309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175G>A
AA Mutation	p.Glu59Lys(p.E59K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374859
Start	32856150:32856150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.73G>A
AA Mutation	p.Ala25Thr(p.A25T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript