Colon Cancer: Gene >> CSRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340006
Start	201488880:201488880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760988527
CDS Mutation	c.386C>T
AA Mutation	p.Ala129Val(p.A129V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340006
Start	201490197:201490197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260C>T
AA Mutation	p.Ser87Leu(p.S87L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340006
Start	201490229:201490229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554244394
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000340006
Start	201485283:201485283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>T
AA Mutation	p.Gly169Ter(p.G169*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CSRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340006
Start	201490289:201490289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168T>G
AA Mutation	p.Ile56Met(p.I56M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000340006
Start	201485355:201485355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772065755
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Ter(p.R145*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript