Colon Cancer: Gene >> PRRG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257836
Start	32840148:32840148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>A
AA Mutation	p.Gly120Arg(p.G120R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257836
Start	32836687:32836687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133T>G
AA Mutation	p.Phe45Val(p.F45V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257836
Start	32853380:32853380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11032025
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRRG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257836
Start	32838889:32838889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275T>G
AA Mutation	p.Phe92Cys(p.F92C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript