Colon Cancer: Gene >> RFFL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315249
Start	35021684:35021684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278C>G
AA Mutation	p.Ala93Gly(p.A93G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315249
Start	35012112:35012112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762391280
CDS Mutation	c.948T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000315249
Start	35016428:35016428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828G>A
AA Mutation	p.Trp276Ter(p.W276*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000315249
Start	35016429:35016429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.827G>A
AA Mutation	p.Trp276Ter(p.W276*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RFFL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315249
Start	35021380:35021380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582G>T
AA Mutation	p.Glu194Asp(p.E194D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	start_lost
Transcription ID	ENST00000315249
Start	35026552:35026552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript