Colon Cancer: Gene >> FAXDC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326080
Start	154823432:154823432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.527C>T
AA Mutation	p.Ala176Val(p.A176V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326080
Start	154822475:154822475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000326080
Start	154820473:154820473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.846-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FAXDC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326080
Start	154830826:154830826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748240055
CDS Mutation	c.341G>A
AA Mutation	p.Arg114Gln(p.R114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326080
Start	154822508:154822508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377379224
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript