Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ROBO2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77098247:77098247(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.295C>T
AA Mutation p.Arg99Cys(p.R99C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77635011:77635011(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3902C>T
AA Mutation p.Ala1301Val(p.A1301V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77481117:77481117(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201584681
CDS Mutation c.565A>G
AA Mutation p.Met189Val(p.M189V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77574602:77574602(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747073426
CDS Mutation c.2075C>T
AA Mutation p.Pro692Leu(p.P692L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77617656:77617656(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3437G>A
AA Mutation p.Gly1146Glu(p.G1146E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77564986:77564986(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1715C>A
AA Mutation p.Ala572Glu(p.A572E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77588824:77588824(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2574A>C
AA Mutation p.Gln858His(p.Q858H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77563188:77563188(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1541A>C
AA Mutation p.Lys514Thr(p.K514T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77574611:77574611(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2084G>A
AA Mutation p.Arg695Gln(p.R695Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77522856:77522856(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.888G>T
AA Mutation p.Glu296Asp(p.E296D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77596695:77596695(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2799G>T
AA Mutation p.Leu933Phe(p.L933F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77596702:77596702(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2806A>C
AA Mutation p.Asn936His(p.N936H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77580008:77580008(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201678507
CDS Mutation c.2390G>A
AA Mutation p.Arg797Gln(p.R797Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77602267:77602267(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2912G>A
AA Mutation p.Gly971Glu(p.G971E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77596691:77596691(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2795G>C
AA Mutation p.Ser932Thr(p.S932T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000461745
Start 77580118:77580118(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2500G>C
AA Mutation p.Gly834Arg(p.G834R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77098130:77098130(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.178C>T
AA Mutation p.Pro60Ser(p.P60S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77563302:77563302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1655C>A
AA Mutation p.Ala552Glu(p.A552E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77577505:77577505(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2219C>G
AA Mutation p.Pro740Arg(p.P740R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77622358:77622358(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3686A>C
AA Mutation p.Glu1229Ala(p.E1229A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000461745
Start 77558147:77558147(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs555617157
CDS Mutation c.1435C>T
AA Mutation p.Arg479Trp(p.R479W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77634993:77634993(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762523752
CDS Mutation c.3884G>A
AA Mutation p.Arg1295Gln(p.R1295Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77579972:77579972(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750182926
CDS Mutation c.2354G>A
AA Mutation p.Arg785Gln(p.R785Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77098310:77098310(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.358G>C
AA Mutation p.Val120Leu(p.V120L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77098122:77098122(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.170G>A
AA Mutation p.Arg57Gln(p.R57Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77622308:77622308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3636G>T
AA Mutation p.Leu1212Phe(p.L1212F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77098076:77098076(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778684665
CDS Mutation c.124G>A
AA Mutation p.Val42Ile(p.V42I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77550905:77550905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1147C>T
AA Mutation p.Arg383Cys(p.R383C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77493273:77493273(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.697A>G
AA Mutation p.Asn233Asp(p.N233D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77562729:77562729(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1516A>G
AA Mutation p.Thr506Ala(p.T506A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77574664:77574664(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773112305
CDS Mutation c.2137C>T
AA Mutation p.Arg713Trp(p.R713W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77477464:77477464(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.439G>C
AA Mutation p.Gly147Arg(p.G147R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77565088:77565088(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778929785
CDS Mutation c.1817C>T
AA Mutation p.Pro606Leu(p.P606L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77588927:77588927(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2677T>G
AA Mutation p.Tyr893Asp(p.Y893D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77634965:77634965(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs62250276
CDS Mutation c.3856C>T
AA Mutation p.Arg1286Trp(p.R1286W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77562687:77562687(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1474A>C
AA Mutation p.Ser492Arg(p.S492R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77607915:77607915(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201486215
CDS Mutation c.3254C>T
AA Mutation p.Thr1085Met(p.T1085M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77481103:77481103(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200483677
CDS Mutation c.551G>A
AA Mutation p.Arg184His(p.R184H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77644821:77644821(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4052C>A
AA Mutation p.Ala1351Glu(p.A1351E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77607890:77607890(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201356083
CDS Mutation c.3229C>G
AA Mutation p.Pro1077Ala(p.P1077A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77622341:77622341(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs2272164
CDS Mutation c.3669C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77098324:77098324(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763736763
CDS Mutation c.372G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77644819:77644819(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4050A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77098129:77098129(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762225187
CDS Mutation c.177G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77617627:77617627(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143561771
CDS Mutation c.3408C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77622338:77622338(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201339466
CDS Mutation c.3666C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77550907:77550907(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1149T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77644825:77644825(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4056C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000461745
Start 77634974:77634974(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3870delA
AA Mutation p.Lys1290AsnfsTer20(p.K1290Nfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000461745
Start 77493351:77493351(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.779delA
AA Mutation p.Lys260ArgfsTer19(p.K260Rfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 51
Mutation Consequence stop_gained
Transcription ID ENST00000461745
Start 77098160:77098160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.208C>T
AA Mutation p.Arg70Ter(p.R70*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000461745
Start 77098316:77098316(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.364C>T
AA Mutation p.Arg122Ter(p.R122*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence stop_gained
Transcription ID ENST00000461745
Start 77477542:77477542(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.517C>T
AA Mutation p.Arg173Ter(p.R173*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence stop_gained
Transcription ID ENST00000461745
Start 77617622:77617622(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3403C>T
AA Mutation p.Arg1135Ter(p.R1135*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 55
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000461745
Start 77595143:77595144(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2686dupA
AA Mutation p.Thr896AsnfsTer23(p.T896Nfs*23)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 56
Mutation Consequence frameshift_variant
Transcription ID ENST00000461745
Start 77607886:77607887(version: GRCh38)
Mutation Type INS
dbSNP_RS rs778666599
CDS Mutation c.3233dupC
AA Mutation p.Val1079SerfsTer22(p.V1079Sfs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 57
Mutation Consequence frameshift_variant
Transcription ID ENST00000461745
Start 77580078:77580079(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2460_2461insT
AA Mutation p.Gly821TrpfsTer7(p.G821Wfs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 58
Mutation Consequence frameshift_variant
Transcription ID ENST00000461745
Start 77546436:77546437(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1039dupT
AA Mutation p.Trp347LeufsTer21(p.W347Lfs*21)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 59
Mutation Consequence frameshift_variant
Transcription ID ENST00000461745
Start 77577498:77577499(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2216dupC
AA Mutation p.Pro740ThrfsTer14(p.P740Tfs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 60
Mutation Consequence splice_donor_variant;intron_variant
Transcription ID ENST00000461745
Start 77588934:77588937(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2683+3_2683+6delAAGT
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 61
Mutation Consequence inframe_insertion
Transcription ID ENST00000461745
Start 77588928:77588929(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2678_2679insCAACTTCAT
AA Mutation p.Tyr893_Ala894insAsnPheIle(p.Y893_A894insNFI)
Mutation Classification In_Frame_Ins
Feature Type Transcript

Rectum Cancer: Gene >> ROBO2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77550911:77550911(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1153G>A
AA Mutation p.Asp385Asn(p.D385N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77098044:77098044(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.92C>T
AA Mutation p.Pro31Leu(p.P31L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77098076:77098076(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778684665
CDS Mutation c.124G>A
AA Mutation p.Val42Ile(p.V42I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77098284:77098284(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.332T>A
AA Mutation p.Val111Asp(p.V111D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77493307:77493307(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.731T>G
AA Mutation p.Phe244Cys(p.F244C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77607827:77607827(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3166A>G
AA Mutation p.Lys1056Glu(p.K1056E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77574575:77574575(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2048C>T
AA Mutation p.Ser683Leu(p.S683L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77602482:77602482(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3127G>C
AA Mutation p.Gly1043Arg(p.G1043R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77546367:77546367(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.964G>T
AA Mutation p.Asp322Tyr(p.D322Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000461745
Start 77564999:77564999(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1728G>T
AA Mutation p.Lys576Asn(p.K576N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77574532:77574532(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375822408
CDS Mutation c.2005C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000461745
Start 77617559:77617559(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3340T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000461745
Start 77588897:77588897(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2647C>T
AA Mutation p.Arg883Ter(p.R883*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000461745
Start 77477542:77477542(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.517C>T
AA Mutation p.Arg173Ter(p.R173*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000461745
Start 77602383:77602383(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3028G>T
AA Mutation p.Glu1010Ter(p.E1010*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000461745
Start 77617622:77617622(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3403C>T
AA Mutation p.Arg1135Ter(p.R1135*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript