Colon Cancer: Gene >> RBFOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000438146
Start	35759979:35759979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018G>A
AA Mutation	p.Ala340Thr(p.A340T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000438146
Start	35768312:35768312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.701C>T
AA Mutation	p.Ala234Val(p.A234V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000438146
Start	35781698:35781698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511A>C
AA Mutation	p.Ser171Arg(p.S171R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000438146
Start	35809950:35809950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292A>T
AA Mutation	p.Ile98Phe(p.I98F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000438146
Start	35809974:35809974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140420879
CDS Mutation	c.268G>A
AA Mutation	p.Ala90Thr(p.A90T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438146
Start	35768290:35768290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RBFOX2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438146
Start	35809828:35809828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750871473
CDS Mutation	c.414C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000438146
Start	35768326:35768326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687G>A
Mutation Classification	Silent
Feature Type	Transcript