Colon Cancer: Gene >> PSMB8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374882
Start	32842249:32842249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Arg141Gln(p.R141Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374882
Start	32841664:32841664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374882
Start	32843966:32843966(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.31delC
AA Mutation	p.Arg11GlufsTer74(p.R11Efs*74)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000374882
Start	32842250:32842250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374929612
CDS Mutation	c.421C>T
AA Mutation	p.Arg141Ter(p.R141*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PSMB8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374882
Start	32840964:32840964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826C>A
AA Mutation	p.Gln276Lys(p.Q276K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374882
Start	32843065:32843065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172G>T
AA Mutation	p.Gly58Cys(p.G58C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374882
Start	32842225:32842225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446C>T
AA Mutation	p.Ser149Leu(p.S149L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript