Colon Cancer: Gene >> PTPRU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29325620:29325620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773558468
CDS Mutation	c.4300G>A
AA Mutation	p.Asp1434Asn(p.D1434N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29315442:29315442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778440993
CDS Mutation	c.3328G>A
AA Mutation	p.Val1110Ile(p.V1110I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29303864:29303864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2516G>A
AA Mutation	p.Arg839His(p.R839H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29282689:29282689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1882A>T
AA Mutation	p.Ile628Phe(p.I628F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29312657:29312657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374116935
CDS Mutation	c.3208G>A
AA Mutation	p.Val1070Met(p.V1070M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29311696:29311696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3039G>T
AA Mutation	p.Lys1013Asn(p.K1013N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29282704:29282704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757579431
CDS Mutation	c.1897C>T
AA Mutation	p.Arg633Trp(p.R633W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29315424:29315424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3310A>T
AA Mutation	p.Met1104Leu(p.M1104L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29282816:29282816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147046605
CDS Mutation	c.2009C>T
AA Mutation	p.Ala670Val(p.A670V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29315385:29315385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760871118
CDS Mutation	c.3271C>T
AA Mutation	p.Arg1091Cys(p.R1091C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29303927:29303927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200085066
CDS Mutation	c.2579G>A
AA Mutation	p.Arg860Gln(p.R860Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29259292:29259292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752228030
CDS Mutation	c.509G>A
AA Mutation	p.Arg170His(p.R170H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29255400:29255400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199C>T
AA Mutation	p.Pro67Ser(p.P67S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29275540:29275540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771686501
CDS Mutation	c.1237C>T
AA Mutation	p.Arg413Cys(p.R413C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29325232:29325232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4184C>T
AA Mutation	p.Thr1395Met(p.T1395M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29284746:29284746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2195G>A
AA Mutation	p.Ser732Asn(p.S732N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29320755:29320755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760809964
CDS Mutation	c.3788G>A
AA Mutation	p.Arg1263Gln(p.R1263Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29320741:29320741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138823810
CDS Mutation	c.3774G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29305401:29305401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374111722
CDS Mutation	c.2823C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29282775:29282775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1968G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29275491:29275491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1188G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29282817:29282817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142462225
CDS Mutation	c.2010G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29304012:29304012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771289142
CDS Mutation	c.2664G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29317846:29317846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377688027
CDS Mutation	c.3642G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29320780:29320780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3813C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29280130:29280130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1857T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29303949:29303949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748568462
CDS Mutation	c.2601G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345512
Start	29303898:29303898(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2555delG
AA Mutation	p.Gly852AlafsTer35(p.G852Afs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345512
Start	29258677:29258677(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.382delC
AA Mutation	p.Leu128TrpfsTer8(p.L128Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345512
Start	29259283:29259283(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.503delC
AA Mutation	p.Pro168GlnfsTer9(p.P168Qfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000345512
Start	29323789:29323789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4142+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PTPRU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29316069:29316069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3461T>C
AA Mutation	p.Val1154Ala(p.V1154A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29325222:29325222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4174G>A
AA Mutation	p.Ala1392Thr(p.A1392T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29316105:29316105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3497G>A
AA Mutation	p.Arg1166His(p.R1166H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29320748:29320748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3781T>C
AA Mutation	p.Phe1261Leu(p.F1261L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29325270:29325270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771500483
CDS Mutation	c.4222G>A
AA Mutation	p.Val1408Ile(p.V1408I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345512
Start	29291913:29291913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2393A>C
AA Mutation	p.Glu798Ala(p.E798A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345512
Start	29260707:29260707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript