Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PTPRZ1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122031525:122031525(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5132T>C
AA Mutation p.Leu1711Ser(p.L1711S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122012559:122012559(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3513G>T
AA Mutation p.Glu1171Asp(p.E1171D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122013054:122013054(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4008T>G
AA Mutation p.Ile1336Met(p.I1336M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122011418:122011418(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2372A>T
AA Mutation p.Asp791Val(p.D791V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122010943:122010943(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1897G>T
AA Mutation p.Asp633Tyr(p.D633Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122013257:122013257(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4211A>G
AA Mutation p.His1404Arg(p.H1404R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122036657:122036657(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5342A>C
AA Mutation p.Asp1781Ala(p.D1781A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122012531:122012531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3485C>A
AA Mutation p.Ser1162Tyr(p.S1162Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122013003:122013003(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3957T>G
AA Mutation p.Ile1319Met(p.I1319M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122012294:122012294(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778883937
CDS Mutation c.3248C>T
AA Mutation p.Ala1083Val(p.A1083V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122059859:122059859(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6778C>A
AA Mutation p.Leu2260Met(p.L2260M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122038862:122038862(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5475G>C
AA Mutation p.Met1825Ile(p.M1825I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122061110:122061110(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6838C>A
AA Mutation p.Leu2280Ile(p.L2280I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122013734:122013734(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4688A>C
AA Mutation p.Glu1563Ala(p.E1563A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122010880:122010880(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1834G>A
AA Mutation p.Glu612Lys(p.E612K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122011405:122011405(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2359G>T
AA Mutation p.Ala787Ser(p.A787S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 121976815:121976815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.583G>T
AA Mutation p.Ala195Ser(p.A195S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 121983809:121983809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.764T>C
AA Mutation p.Ile255Thr(p.I255T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122055021:122055021(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6462A>C
AA Mutation p.Glu2154Asp(p.E2154D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122013365:122013365(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139890527
CDS Mutation c.4319A>G
AA Mutation p.His1440Arg(p.H1440R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122011915:122011915(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2869A>G
AA Mutation p.Thr957Ala(p.T957A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 121997973:121997973(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1207C>G
AA Mutation p.Gln403Glu(p.Q403E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122012621:122012621(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3575A>G
AA Mutation p.Asp1192Gly(p.D1192G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122010605:122010605(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1559C>A
AA Mutation p.Ser520Tyr(p.S520Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122010897:122010897(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1851A>G
AA Mutation p.Ile617Met(p.I617M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000393386
Start 122036602:122036602(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5287G>T
AA Mutation p.Asp1763Tyr(p.D1763Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122012225:122012225(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs529791225
CDS Mutation c.3179A>G
AA Mutation p.Asn1060Ser(p.N1060S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122010589:122010589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1543G>A
AA Mutation p.Asp515Asn(p.D515N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122011543:122011543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760236914
CDS Mutation c.2497C>T
AA Mutation p.Arg833Cys(p.R833C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122011456:122011456(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2410G>C
AA Mutation p.Asp804His(p.D804H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122011733:122011733(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2687C>A
AA Mutation p.Ser896Tyr(p.S896Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122013074:122013074(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4028C>A
AA Mutation p.Ser1343Tyr(p.S1343Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 121976846:121976846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.614G>A
AA Mutation p.Arg205His(p.R205H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122010577:122010577(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1531G>A
AA Mutation p.Ala511Thr(p.A511T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122013825:122013825(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4779C>A
AA Mutation p.Phe1593Leu(p.F1593L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122010513:122010513(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1467C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 121997903:121997903(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1137A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122042686:122042686(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772395547
CDS Mutation c.5880C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122011917:122011917(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2871T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122013468:122013468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4422A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 121984089:121984089(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.900C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 121983753:121983753(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.708A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122040905:122040905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5727G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122013297:122013297(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4251A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122042621:122042621(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5815A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000393386
Start 121967963:121967963(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.143delA
AA Mutation p.Asn48IlefsTer26(p.N48Ifs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000393386
Start 121983974:121983974(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.790delT
AA Mutation p.Cys264ValfsTer14(p.C264Vfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 48
Mutation Consequence stop_gained
Transcription ID ENST00000393386
Start 121976176:121976176(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.460C>T
AA Mutation p.Gln154Ter(p.Q154*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000393386
Start 122058799:122058799(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6529-1G>T
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> PTPRZ1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 121968127:121968127(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779912145
CDS Mutation c.301A>G
AA Mutation p.Thr101Ala(p.T101A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122012559:122012559(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3513G>T
AA Mutation p.Glu1171Asp(p.E1171D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122013483:122013483(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4437G>T
AA Mutation p.Glu1479Asp(p.E1479D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000393386
Start 122053911:122053911(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6254G>A
AA Mutation p.Gly2085Asp(p.G2085D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122011543:122011543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760236914
CDS Mutation c.2497C>T
AA Mutation p.Arg833Cys(p.R833C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122059868:122059868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6787C>T
AA Mutation p.Pro2263Ser(p.P2263S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122011523:122011523(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2477C>T
AA Mutation p.Ser826Phe(p.S826F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122010946:122010946(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1900T>G
AA Mutation p.Ser634Ala(p.S634A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122059760:122059760(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6679G>A
AA Mutation p.Gly2227Arg(p.G2227R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122011594:122011594(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756306704
CDS Mutation c.2548G>A
AA Mutation p.Glu850Lys(p.E850K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122012570:122012570(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746282121
CDS Mutation c.3524C>A
AA Mutation p.Ser1175Tyr(p.S1175Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122053975:122053975(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6318C>A
AA Mutation p.Phe2106Leu(p.F2106L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 121976846:121976846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.614G>A
AA Mutation p.Arg205His(p.R205H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 121967967:121967967(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.141A>C
AA Mutation p.Lys47Asn(p.K47N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000393386
Start 122051496:122051496(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6153G>T
AA Mutation p.Lys2051Asn(p.K2051N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122012961:122012961(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3915C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122012658:122012658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3612T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122011146:122011146(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2100A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000393386
Start 122019179:122019179(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778664781
CDS Mutation c.4899C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence stop_gained
Transcription ID ENST00000393386
Start 121984045:121984045(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771283585
CDS Mutation c.856C>T
AA Mutation p.Arg286Ter(p.R286*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript