Colon Cancer: Gene >> NCL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322723
Start	231459078:231459078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1088C>T
AA Mutation	p.Ala363Val(p.A363V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322723
Start	231456064:231456064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1778A>G
AA Mutation	p.Asp593Gly(p.D593G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322723
Start	231460734:231460734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112363453
CDS Mutation	c.746A>G
AA Mutation	p.Asp249Gly(p.D249G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000322723
Start	231460865:231460865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.615C>A
AA Mutation	p.Asp205Glu(p.D205E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322723
Start	231460552:231460552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824A>T
AA Mutation	p.Glu275Val(p.E275V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322723
Start	231461577:231461577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767449678
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322723
Start	231459053:231459053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322723
Start	231458304:231458304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546418951
CDS Mutation	c.1251G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322723
Start	231455498:231455498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762540059
CDS Mutation	c.1959C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000322723
Start	231463255:231463257(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs752943861
CDS Mutation	c.78_80delAGA
AA Mutation	p.Glu26del(p.E26del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NCL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322723
Start	231456031:231456031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1811G>A
AA Mutation	p.Arg604Gln(p.R604Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322723
Start	231459053:231459053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1113C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322723
Start	231461700:231461700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000322723
Start	231460701:231460703(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746082903
CDS Mutation	c.777_779delAGA
AA Mutation	p.Glu259del(p.E259del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript