Colon Cancer: Gene >> CTSG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216336
Start	24574294:24574294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545G>A
AA Mutation	p.Arg182Gln(p.R182Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216336
Start	24575313:24575313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155T>G
AA Mutation	p.Phe52Cys(p.F52C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216336
Start	24573757:24573757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216336
Start	24574741:24574741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000216336
Start	24574475:24574475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Ter(p.R122*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CTSG

No Mutation Annotation!