Colon Cancer: Gene >> COPB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139374516:139374516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724C>T
AA Mutation	p.Pro242Ser(p.P242S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139383422:139383422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.17A>G
AA Mutation	p.Asp6Gly(p.D6G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139361101:139361101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2190G>C
AA Mutation	p.Met730Ile(p.M730I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000333188
Start	139378188:139378188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357T>G
AA Mutation	p.Asp119Glu(p.D119E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139373246:139373246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061A>G
AA Mutation	p.Tyr354Cys(p.Y354C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139375571:139375571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.548G>A
AA Mutation	p.Gly183Glu(p.G183E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139379426:139379426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182G>A
AA Mutation	p.Arg61Gln(p.R61Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139379430:139379430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178G>A
AA Mutation	p.Val60Ile(p.V60I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139369483:139369483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1267T>A
AA Mutation	p.Ser423Thr(p.S423T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139379095:139379095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307C>T
AA Mutation	p.Arg103Cys(p.R103C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333188
Start	139373732:139373732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776384424
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> COPB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139378167:139378167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>C
AA Mutation	p.Trp126Cys(p.W126C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139373701:139373701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771486381
CDS Mutation	c.859G>A
AA Mutation	p.Ala287Thr(p.A287T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333188
Start	139371759:139371759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1169C>T
AA Mutation	p.Ser390Phe(p.S390F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333188
Start	139373801:139373801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.759A>G
Mutation Classification	Silent
Feature Type	Transcript