Colon Cancer: Gene >> USP15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62321551:62321551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563T>G
AA Mutation	p.Phe188Cys(p.F188C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62396360:62396360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2636C>T
AA Mutation	p.Ala879Val(p.A879V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62384124:62384124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1295C>A
AA Mutation	p.Ser432Tyr(p.S432Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62321477:62321477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489G>T
AA Mutation	p.Lys163Asn(p.K163N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62404277:62404277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2848G>T
AA Mutation	p.Gly950Cys(p.G950C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62302808:62302808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236T>G
AA Mutation	p.Leu79Arg(p.L79R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62393157:62393157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2525G>A
AA Mutation	p.Arg842Gln(p.R842Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62302871:62302871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299T>G
AA Mutation	p.Leu100Arg(p.L100R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62391247:62391247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2051T>G
AA Mutation	p.Val684Gly(p.V684G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62383956:62383956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206A>C
AA Mutation	p.Lys402Asn(p.K402N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62384115:62384115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429Gln(p.R429Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62389617:62389617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1570G>C
AA Mutation	p.Asp524His(p.D524H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62389650:62389650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367863159
CDS Mutation	c.1603G>A
AA Mutation	p.Ala535Thr(p.A535T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000280377
Start	62314870:62314870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280377
Start	62404250:62404250(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2826delT
AA Mutation	p.Pro943LeufsTer17(p.P943Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280377
Start	62384240:62384240(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1416delA
AA Mutation	p.Glu473AsnfsTer8(p.E473Nfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280377
Start	62391853:62391854(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2278dupA
AA Mutation	p.Arg760LysfsTer4(p.R760Kfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000280377
Start	62383950:62383951(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1206dupA
AA Mutation	p.Pro403ThrfsTer14(p.P403Tfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000280377
Start	62389796:62389796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1653-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> USP15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62355390:62355390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774222038
CDS Mutation	c.830C>T
AA Mutation	p.Ser277Leu(p.S277L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62396309:62396309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754226149
CDS Mutation	c.2585C>T
AA Mutation	p.Ser862Leu(p.S862L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000280377
Start	62383869:62383869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119C>A
AA Mutation	p.Phe373Leu(p.F373L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript