Colon Cancer: Gene >> SCTR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000019103
Start	119464147:119464147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612T>G
AA Mutation	p.Asp204Glu(p.D204E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000019103
Start	119473506:119473506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352A>G
AA Mutation	p.Arg118Gly(p.R118G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000019103
Start	119478868:119478868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244G>A
AA Mutation	p.Gly82Ser(p.G82S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000019103
Start	119473454:119473454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404G>A
AA Mutation	p.Arg135Gln(p.R135Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000019103
Start	119464170:119464170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779937018
CDS Mutation	c.589G>A
AA Mutation	p.Ala197Thr(p.A197T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000019103
Start	119452036:119452036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144810736
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Cys(p.R299C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000019103
Start	119494461:119494461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160A>G
AA Mutation	p.Thr54Ala(p.T54A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000019103
Start	119473507:119473507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000019103
Start	119494509:119494509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000019103
Start	119446825:119446825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140245245
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000019103
Start	119478890:119478890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000019103
Start	119494464:119494464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157C>T
AA Mutation	p.Gln53Ter(p.Q53*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SCTR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000019103
Start	119464238:119464238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748166802
CDS Mutation	c.521G>A
AA Mutation	p.Arg174His(p.R174H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000019103
Start	119461854:119461854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766336754
CDS Mutation	c.783C>T
Mutation Classification	Silent
Feature Type	Transcript