Colon Cancer: Gene >> GSC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238558
Start	94769058:94769058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515T>G
AA Mutation	p.Leu172Arg(p.L172R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000238558
Start	94769098:94769098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475C>T
AA Mutation	p.Arg159Trp(p.R159W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000238558
Start	94768972:94768972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601G>A
AA Mutation	p.Glu201Lys(p.E201K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000238558
Start	94769188:94769188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.385T>C
AA Mutation	p.Ser129Pro(p.S129P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GSC

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238558
Start	94769024:94769024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.549G>A
Mutation Classification	Silent
Feature Type	Transcript