Colon Cancer: Gene >> USP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260187
Start	119373031:119373031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450C>A
AA Mutation	p.Phe150Leu(p.F150L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260187
Start	119372855:119372855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626C>A
AA Mutation	p.Ser209Tyr(p.S209Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260187
Start	119372753:119372753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728A>G
AA Mutation	p.Gln243Arg(p.Q243R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260187
Start	119357229:119357229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756703374
CDS Mutation	c.1688G>A
AA Mutation	p.Arg563His(p.R563H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260187
Start	119373194:119373194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287C>T
AA Mutation	p.Thr96Ile(p.T96I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260187
Start	119357239:119357239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1678G>A
AA Mutation	p.Ala560Thr(p.A560T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260187
Start	119356895:119356895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1758G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260187
Start	119373007:119373007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769234434
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260187
Start	119359248:119359248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143916320
CDS Mutation	c.1044G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> USP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260187
Start	119359256:119359256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1036T>C
AA Mutation	p.Tyr346His(p.Y346H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260187
Start	119357582:119357582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1510C>T
AA Mutation	p.Arg504Trp(p.R504W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260187
Start	119358179:119358179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1311C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000260187
Start	119357504:119357504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1588G>T
AA Mutation	p.Glu530Ter(p.E530*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript