Colon Cancer: Gene >> MRGPRF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309099
Start	69005984:69005984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.326G>A
AA Mutation	p.Gly109Asp(p.G109D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309099
Start	69005846:69005846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.464G>T
AA Mutation	p.Arg155Leu(p.R155L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309099
Start	69005488:69005488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144312357
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309099
Start	69005683:69005683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.627C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309099
Start	69006049:69006049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774832812
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MRGPRF

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309099
Start	69005455:69005455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.855C>T
Mutation Classification	Silent
Feature Type	Transcript