Colon Cancer: Gene >> NOVA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263257
Start	45940423:45940423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.919G>A
AA Mutation	p.Gly307Ser(p.G307S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263257
Start	45939979:45939979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1363C>T
AA Mutation	p.Arg455Trp(p.R455W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263257
Start	45953890:45953890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286C>A
AA Mutation	p.His96Asn(p.H96N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263257
Start	45939985:45939985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357C>T
AA Mutation	p.Arg453Trp(p.R453W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263257
Start	45940876:45940876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200399286
CDS Mutation	c.466G>A
AA Mutation	p.Val156Met(p.V156M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263257
Start	45940412:45940412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263257
Start	45940892:45940892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263257
Start	45940919:45940919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368021609
CDS Mutation	c.423G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263257
Start	45961074:45961074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263257
Start	45961110:45961110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NOVA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263257
Start	45940693:45940693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754714738
CDS Mutation	c.649G>A
AA Mutation	p.Val217Met(p.V217M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263257
Start	45940733:45940733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609C>A
AA Mutation	p.Asp203Glu(p.D203E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263257
Start	45939953:45939953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263257
Start	45940754:45940754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.588C>T
Mutation Classification	Silent
Feature Type	Transcript