Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PLXND1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129565407:129565407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4454G>A
AA Mutation p.Arg1485His(p.R1485H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129567703:129567703(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3968G>A
AA Mutation p.Arg1323His(p.R1323H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129586626:129586626(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1582G>A
AA Mutation p.Ala528Thr(p.A528T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129570812:129570812(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140631068
CDS Mutation c.3724G>A
AA Mutation p.Ala1242Thr(p.A1242T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129565411:129565411(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4450C>T
AA Mutation p.Arg1484Trp(p.R1484W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129571762:129571762(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761956464
CDS Mutation c.3160C>T
AA Mutation p.Arg1054Trp(p.R1054W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129584484:129584484(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767575252
CDS Mutation c.1930C>T
AA Mutation p.Arg644Cys(p.R644C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129569947:129569947(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3761G>A
AA Mutation p.Gly1254Glu(p.G1254E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129574458:129574458(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775216644
CDS Mutation c.2563G>A
AA Mutation p.Asp855Asn(p.D855N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129561849:129561849(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4880C>T
AA Mutation p.Ser1627Leu(p.S1627L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129558496:129558496(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5377G>A
AA Mutation p.Ala1793Thr(p.A1793T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129557156:129557156(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5513A>G
AA Mutation p.Tyr1838Cys(p.Y1838C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129569854:129569854(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3854T>C
AA Mutation p.Leu1285Pro(p.L1285P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129583592:129583592(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138740853
CDS Mutation c.2216G>A
AA Mutation p.Arg739Gln(p.R739Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129556661:129556661(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5617G>A
AA Mutation p.Ala1873Thr(p.A1873T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129606458:129606458(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.182A>G
AA Mutation p.Asn61Ser(p.N61S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129556422:129556422(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5668G>A
AA Mutation p.Ala1890Thr(p.A1890T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129560347:129560347(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746921963
CDS Mutation c.5116C>T
AA Mutation p.Arg1706Cys(p.R1706C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129575549:129575549(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141279701
CDS Mutation c.2450G>A
AA Mutation p.Arg817Gln(p.R817Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129560424:129560424(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs569800532
CDS Mutation c.5039C>T
AA Mutation p.Thr1680Met(p.T1680M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129559779:129559779(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5138C>T
AA Mutation p.Thr1713Met(p.T1713M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129565509:129565509(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368069685
CDS Mutation c.4352C>T
AA Mutation p.Ala1451Val(p.A1451V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129571825:129571825(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3097G>A
AA Mutation p.Ala1033Thr(p.A1033T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129586175:129586175(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151013320
CDS Mutation c.1718C>T
AA Mutation p.Thr573Met(p.T573M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129558517:129558517(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751152442
CDS Mutation c.5356G>A
AA Mutation p.Asp1786Asn(p.D1786N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129565430:129565430(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4431G>T
AA Mutation p.Lys1477Asn(p.K1477N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129572900:129572900(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2879G>A
AA Mutation p.Gly960Asp(p.G960D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129567553:129567553(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769351907
CDS Mutation c.4025G>A
AA Mutation p.Arg1342His(p.R1342H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129558534:129558534(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5339A>G
AA Mutation p.Gln1780Arg(p.Q1780R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129584419:129584419(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141599469
CDS Mutation c.1995G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129556620:129556620(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755134184
CDS Mutation c.5658G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129571132:129571132(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3508C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129556399:129556399(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761700156
CDS Mutation c.5691G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129566587:129566587(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4131C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129560411:129560411(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200333536
CDS Mutation c.5052G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129572617:129572617(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs561945149
CDS Mutation c.3069G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129589387:129589387(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763302268
CDS Mutation c.1452G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129556638:129556638(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs542768361
CDS Mutation c.5640C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129606220:129606220(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.420C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129570831:129570831(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762034293
CDS Mutation c.3705G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129572704:129572704(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs113382224
CDS Mutation c.2982C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129565436:129565436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs189832202
CDS Mutation c.4425C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129566566:129566566(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4152C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129557191:129557191(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5478G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129605932:129605932(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.708C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129573656:129573656(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370338586
CDS Mutation c.2775C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129557128:129557128(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs571320102
CDS Mutation c.5541G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000324093
Start 129584392:129584392(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2022delC
AA Mutation p.Asn675ThrfsTer5(p.N675Tfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000324093
Start 129575790:129575791(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2411_2412delCT
AA Mutation p.Ser804CysfsTer5(p.S804Cfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000324093
Start 129556402:129556402(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5688delC
AA Mutation p.Thr1897ArgfsTer17(p.T1897Rfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 51
Mutation Consequence frameshift_variant
Transcription ID ENST00000324093
Start 129559716:129559716(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5201delC
AA Mutation p.Pro1734HisfsTer40(p.P1734Hfs*40)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000324093
Start 129573697:129573697(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2734C>T
AA Mutation p.Arg912Ter(p.R912*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence frameshift_variant
Transcription ID ENST00000324093
Start 129569907:129569908(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.3800dupG
AA Mutation p.Ser1268GlnfsTer34(p.S1268Qfs*34)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> PLXND1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129571716:129571716(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779527122
CDS Mutation c.3206C>T
AA Mutation p.Pro1069Leu(p.P1069L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129585965:129585965(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773387450
CDS Mutation c.1838G>A
AA Mutation p.Arg613His(p.R613H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129574436:129574436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745841532
CDS Mutation c.2585G>A
AA Mutation p.Arg862His(p.R862H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000324093
Start 129571842:129571842(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754831143
CDS Mutation c.3080G>A
AA Mutation p.Arg1027His(p.R1027H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129571134:129571134(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200890421
CDS Mutation c.3506G>A
AA Mutation p.Arg1169His(p.R1169H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129589476:129589476(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1363T>C
AA Mutation p.Ser455Pro(p.S455P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000324093
Start 129605941:129605941(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.699G>T
AA Mutation p.Glu233Asp(p.E233D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129583609:129583609(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2199T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129570903:129570903(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs552585270
CDS Mutation c.3633C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129558518:129558518(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149756843
CDS Mutation c.5355C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000324093
Start 129572644:129572644(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3042C>A
Mutation Classification Silent
Feature Type Transcript