Colon Cancer: Gene >> CDC40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307731
Start	110213093:110213093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875G>A
AA Mutation	p.Ser292Asn(p.S292N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307731
Start	110228919:110228919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779945821
CDS Mutation	c.1505T>G
AA Mutation	p.Phe502Cys(p.F502C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307731
Start	110217798:110217798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1085A>C
AA Mutation	p.Glu362Ala(p.E362A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307731
Start	110215295:110215295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>T
AA Mutation	p.Val318Phe(p.V318F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307731
Start	110201627:110201627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375400280
CDS Mutation	c.346G>A
AA Mutation	p.Glu116Lys(p.E116K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307731
Start	110212244:110212244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839A>G
AA Mutation	p.Gln280Arg(p.Q280R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307731
Start	110180479:110180479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.35A>G
AA Mutation	p.Tyr12Cys(p.Y12C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307731
Start	110201573:110201573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292C>A
AA Mutation	p.Pro98Thr(p.P98T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000307731
Start	110210719:110210719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643G>T
AA Mutation	p.Glu215Ter(p.E215*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307731
Start	110210748:110210749(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.678dupA
AA Mutation	p.Gly227ArgfsTer18(p.G227Rfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDC40

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307731
Start	110228887:110228887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1473G>T
AA Mutation	p.Gln491His(p.Q491H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307731
Start	110212249:110212249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844C>A
AA Mutation	p.His282Asn(p.H282N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript