Colon Cancer: Gene >> CFLAR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309955
Start	201160515:201160515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>A
AA Mutation	p.Leu293Ile(p.L293I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309955
Start	201160441:201160441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803G>A
AA Mutation	p.Arg268Gln(p.R268Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309955
Start	201160781:201160781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1143G>T
AA Mutation	p.Lys381Asn(p.K381N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309955
Start	201130042:201130042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.177C>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CFLAR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309955
Start	201145424:201145424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.653G>A
AA Mutation	p.Gly218Asp(p.G218D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309955
Start	201129988:201129988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123G>C
Mutation Classification	Silent
Feature Type	Transcript