Colon Cancer: Gene >> NGDN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000408901
Start	23476355:23476355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763908852
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Cys(p.R221C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000408901
Start	23478012:23478012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199979035
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Trp(p.R312W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000408901
Start	23477251:23477251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.765G>T
AA Mutation	p.Glu255Asp(p.E255D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408901
Start	23478020:23478020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408901
Start	23475733:23475733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000408901
Start	23475780:23475780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.420+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NGDN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000408901
Start	23476039:23476039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431A>T
AA Mutation	p.Glu144Val(p.E144V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript