Colon Cancer: Gene >> CNP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393892
Start	41968714:41968714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650A>G
AA Mutation	p.Lys217Arg(p.K217R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393892
Start	41973631:41973631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199970993
CDS Mutation	c.973C>T
AA Mutation	p.Arg325Trp(p.R325W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393892
Start	41973506:41973506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782078035
CDS Mutation	c.848C>T
AA Mutation	p.Thr283Met(p.T283M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393892
Start	41968693:41968693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629T>C
AA Mutation	p.Leu210Pro(p.L210P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393892
Start	41968084:41968084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20G>A
AA Mutation	p.Arg7Gln(p.R7Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393892
Start	41968735:41968735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671G>A
AA Mutation	p.Arg224Gln(p.R224Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393892
Start	41968310:41968310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782433665
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393892
Start	41973552:41973552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.894C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393892
Start	41968679:41968679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000393892
Start	41968609:41968611(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.547_549delAAG
AA Mutation	p.Lys183del(p.K183del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CNP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393892
Start	41968444:41968444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380A>C
AA Mutation	p.Glu127Ala(p.E127A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript