Colon Cancer: Gene >> USP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8930383:8930383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94G>C
AA Mutation	p.Asp32His(p.D32H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8904542:8904542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374207468
CDS Mutation	c.1597G>A
AA Mutation	p.Asp533Asn(p.D533N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8895649:8895649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2912G>A
AA Mutation	p.Arg971Gln(p.R971Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8923294:8923294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304A>C
AA Mutation	p.Met102Leu(p.M102L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8899620:8899620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2447G>T
AA Mutation	p.Arg816Ile(p.R816I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8910765:8910765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141G>A
AA Mutation	p.Ala381Thr(p.A381T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8895060:8895060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3010G>A
AA Mutation	p.Gly1004Arg(p.G1004R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8894038:8894038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3269G>A
AA Mutation	p.Arg1090His(p.R1090H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000344836
Start	8920359:8920359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611C>T
AA Mutation	p.Ala204Val(p.A204V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8898628:8898628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2543G>T
AA Mutation	p.Gly848Val(p.G848V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8899720:8899720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2347G>A
AA Mutation	p.Ala783Thr(p.A783T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8923320:8923320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.278G>A
AA Mutation	p.Arg93Gln(p.R93Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8904545:8904545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1594A>G
AA Mutation	p.Thr532Ala(p.T532A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8895096:8895096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2974G>A
AA Mutation	p.Val992Met(p.V992M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8910767:8910767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1139A>G
AA Mutation	p.Asp380Gly(p.D380G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8895091:8895091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757705172
CDS Mutation	c.2979G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8903355:8903355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374321309
CDS Mutation	c.1752C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8902182:8902182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113373249
CDS Mutation	c.1947T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8895714:8895714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2847C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8919069:8919069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000344836
Start	8904506:8904506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1633C>T
AA Mutation	p.Gln545Ter(p.Q545*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000344836
Start	8895150:8895150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2920G>T
AA Mutation	p.Glu974Ter(p.E974*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000344836
Start	8902461:8902461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1861C>T
AA Mutation	p.Arg621Ter(p.R621*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000344836
Start	8906578:8906578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276G>T
AA Mutation	p.Glu426Ter(p.E426*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000344836
Start	8923321:8923321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277C>T
AA Mutation	p.Arg93Ter(p.R93*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344836
Start	8906535:8906536(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1318dupA
AA Mutation	p.Thr440AsnfsTer4(p.T440Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> USP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8900548:8900548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2291A>G
AA Mutation	p.Asp764Gly(p.D764G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8894007:8894007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3300C>G
AA Mutation	p.Ile1100Met(p.I1100M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344836
Start	8923287:8923287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311G>A
AA Mutation	p.Arg104His(p.R104H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8898564:8898564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2607G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344836
Start	8906516:8906516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1338A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000344836
Start	8921195:8921195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484G>T
AA Mutation	p.Glu162Ter(p.E162*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript