Colon Cancer: Gene >> USP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63574125:63574125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988G>A
AA Mutation	p.Glu330Lys(p.E330K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63588798:63588798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1312A>G
AA Mutation	p.Lys438Glu(p.K438E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63570564:63570564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.893G>A
AA Mutation	p.Ser298Asn(p.S298N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63590728:63590728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1465A>G
AA Mutation	p.Thr489Ala(p.T489A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63588314:63588314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754082267
CDS Mutation	c.1106G>A
AA Mutation	p.Arg369His(p.R369H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63570452:63570452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>A
AA Mutation	p.Ala261Thr(p.A261T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63588354:63588354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146A>C
AA Mutation	p.Leu382Phe(p.L382F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63588356:63588356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1148A>T
AA Mutation	p.Tyr383Phe(p.Y383F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63570495:63570495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824A>G
AA Mutation	p.Glu275Gly(p.E275G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63570485:63570485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814C>A
AA Mutation	p.Leu272Ile(p.L272I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63588378:63588378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1170G>T
AA Mutation	p.Lys390Asn(p.K390N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63574068:63574068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931A>G
AA Mutation	p.Thr311Ala(p.T311A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380324
Start	63537042:63537043(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.177dupA
AA Mutation	p.His60ThrfsTer3(p.H60Tfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> USP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380324
Start	63553787:63553787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.357G>T
AA Mutation	p.Gln119His(p.Q119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript