Colon Cancer: Gene >> CPXCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753932:88753932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518T>C
AA Mutation	p.Val173Ala(p.V173A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753448:88753448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34G>A
AA Mutation	p.Ala12Thr(p.A12T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753710:88753710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296A>C
AA Mutation	p.Lys99Thr(p.K99T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753464:88753464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.50A>G
AA Mutation	p.Lys17Arg(p.K17R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753947:88753947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533T>C
AA Mutation	p.Ile178Thr(p.I178T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753746:88753746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332G>T
AA Mutation	p.Arg111Ile(p.R111I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753647:88753647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.233A>T
AA Mutation	p.Lys78Ile(p.K78I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88754043:88754043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629A>T
AA Mutation	p.Glu210Val(p.E210V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88754084:88754084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670A>G
AA Mutation	p.Lys224Glu(p.K224E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753848:88753848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434G>A
AA Mutation	p.Ser145Asn(p.S145N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88754031:88754031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144908642
CDS Mutation	c.617G>A
AA Mutation	p.Arg206His(p.R206H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753473:88753473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.59A>C
AA Mutation	p.Glu20Ala(p.E20A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753449:88753449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.35C>T
AA Mutation	p.Ala12Val(p.A12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753992:88753992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754987127
CDS Mutation	c.578C>T
AA Mutation	p.Ala193Val(p.A193V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276127
Start	88753720:88753720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276127
Start	88753567:88753567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276127
Start	88753921:88753921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276127
Start	88754125:88754125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000276127
Start	88753655:88753655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753571924
CDS Mutation	c.241C>T
AA Mutation	p.Arg81Ter(p.R81*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CPXCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88754102:88754102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191294021
CDS Mutation	c.688C>T
AA Mutation	p.Arg230Cys(p.R230C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88754304:88754304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890G>T
AA Mutation	p.Ser297Ile(p.S297I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276127
Start	88753718:88753718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304T>G
AA Mutation	p.Ser102Ala(p.S102A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276127
Start	88753495:88753495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.81T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276127
Start	88753804:88753804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000276127
Start	88753694:88753695(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.285dupC
AA Mutation	p.Ile96HisfsTer13(p.I96Hfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript