Colon Cancer: Gene >> PTGES2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338961
Start	128122412:128122412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.955G>T
AA Mutation	p.Gly319Cys(p.G319C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338961
Start	128125425:128125425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199848207
CDS Mutation	c.296G>A
AA Mutation	p.Arg99His(p.R99H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338961
Start	128122973:128122973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.848C>T
AA Mutation	p.Ala283Val(p.A283V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338961
Start	128121229:128121229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757949315
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTGES2

No Mutation Annotation!