Colon Cancer: Gene >> GRASP

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000293662
Start	52013687:52013687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455G>T
AA Mutation	p.Gly152Val(p.G152V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293662
Start	52013727:52013727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376034891
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000293662
Start	52011105:52011105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>T
AA Mutation	p.Glu140Ter(p.E140*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000293662
Start	52013737:52013737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367922208
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Ter(p.R169*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GRASP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293662
Start	52014189:52014189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670C>T
AA Mutation	p.Arg224Trp(p.R224W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript