Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DCC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53391709:53391709(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2510T>C
AA Mutation p.Val837Ala(p.V837A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53207746:53207746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1790G>A
AA Mutation p.Arg597Gln(p.R597Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53397373:53397373(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2754C>A
AA Mutation p.Phe918Leu(p.F918L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 52906275:52906275(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs112433088
CDS Mutation c.644G>A
AA Mutation p.Arg215Gln(p.R215Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 52906245:52906245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.614G>A
AA Mutation p.Gly205Glu(p.G205E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53305627:53305627(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1961T>G
AA Mutation p.Phe654Cys(p.F654C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53157443:53157443(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780738407
CDS Mutation c.1349G>A
AA Mutation p.Arg450His(p.R450H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53339753:53339753(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2205G>T
AA Mutation p.Arg735Ser(p.R735S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53391765:53391765(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2566A>G
AA Mutation p.Thr856Ala(p.T856A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53178984:53178984(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1441C>A
AA Mutation p.Gln481Lys(p.Q481K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 52752351:52752351(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367734161
CDS Mutation c.389G>A
AA Mutation p.Arg130Gln(p.R130Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53207763:53207763(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs267605206
CDS Mutation c.1807C>T
AA Mutation p.Arg603Cys(p.R603C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53467923:53467923(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3649A>G
AA Mutation p.Met1217Val(p.M1217V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53402797:53402797(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2839G>T
AA Mutation p.Ala947Ser(p.A947S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53305629:53305629(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1963A>T
AA Mutation p.Ile655Phe(p.I655F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 52340853:52340853(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.66G>T
AA Mutation p.Leu22Phe(p.L22F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53467998:53467998(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753205462
CDS Mutation c.3724T>C
AA Mutation p.Ser1242Pro(p.S1242P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53207727:53207727(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1771T>A
AA Mutation p.Phe591Ile(p.F591I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53066134:53066134(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1229A>G
AA Mutation p.Gln410Arg(p.Q410R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53386081:53386081(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2398A>G
AA Mutation p.Asn800Asp(p.N800D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53450641:53450641(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs566224982
CDS Mutation c.3371G>A
AA Mutation p.Arg1124His(p.R1124H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53486811:53486811(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3751A>G
AA Mutation p.Ile1251Val(p.I1251V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53215584:53215584(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1898T>C
AA Mutation p.Val633Ala(p.V633A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 52752084:52752084(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202005334
CDS Mutation c.122G>A
AA Mutation p.Arg41His(p.R41H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53486824:53486824(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775848107
CDS Mutation c.3764C>T
AA Mutation p.Thr1255Met(p.T1255M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53066131:53066131(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776292641
CDS Mutation c.1226C>T
AA Mutation p.Ala409Val(p.A409V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53205224:53205224(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1582C>A
AA Mutation p.Pro528Thr(p.P528T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53157403:53157403(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1309C>A
AA Mutation p.Pro437Thr(p.P437T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 52752359:52752359(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.397A>C
AA Mutation p.Lys133Gln(p.K133Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53499373:53499373(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3974A>T
AA Mutation p.Glu1325Val(p.E1325V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 52923775:52923775(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759718173
CDS Mutation c.766G>A
AA Mutation p.Asp256Asn(p.D256N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53339844:53339844(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2296A>C
AA Mutation p.Ser766Arg(p.S766R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53063374:53063374(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1055G>A
AA Mutation p.Cys352Tyr(p.C352Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53450589:53450589(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3319G>T
AA Mutation p.Gly1107Cys(p.G1107C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53391823:53391823(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747051148
CDS Mutation c.2624C>T
AA Mutation p.Thr875Met(p.T875M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53178974:53178974(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1431G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53397376:53397376(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144874430
CDS Mutation c.2757G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53486849:53486849(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3789A>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53467967:53467967(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3693G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 52340862:52340862(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.75G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53499326:53499326(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3927A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 52752319:52752319(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.357A>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53397331:53397331(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2712T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53410558:53410558(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3042T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53205280:53205280(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1638T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53063309:53063309(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367883098
CDS Mutation c.990G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53322132:53322132(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2139A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence stop_gained
Transcription ID ENST00000442544
Start 53063364:53063364(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1045G>T
AA Mutation p.Glu349Ter(p.E349*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence stop_gained
Transcription ID ENST00000442544
Start 52906070:52906070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.439G>T
AA Mutation p.Glu147Ter(p.E147*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 50
Mutation Consequence stop_gained
Transcription ID ENST00000442544
Start 53499408:53499408(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773315729
CDS Mutation c.4009C>T
AA Mutation p.Arg1337Ter(p.R1337*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 51
Mutation Consequence stop_gained
Transcription ID ENST00000442544
Start 53322106:53322106(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2113G>T
AA Mutation p.Gly705Ter(p.G705*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> DCC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 52925286:52925286(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.901A>G
AA Mutation p.Thr301Ala(p.T301A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53467954:53467954(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762821495
CDS Mutation c.3680G>A
AA Mutation p.Arg1227His(p.R1227H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53157397:53157397(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1303G>A
AA Mutation p.Val435Met(p.V435M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53207727:53207727(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1771T>A
AA Mutation p.Phe591Ile(p.F591I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53339809:53339809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2261T>C
AA Mutation p.Val754Ala(p.V754A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 52752102:52752102(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.140C>A
AA Mutation p.Ser47Tyr(p.S47Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53063315:53063315(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.996G>T
AA Mutation p.Trp332Cys(p.W332C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53157458:53157458(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145985306
CDS Mutation c.1364C>T
AA Mutation p.Ala455Val(p.A455V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 52752200:52752200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.238C>A
AA Mutation p.His80Asn(p.H80N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000442544
Start 53157383:53157383(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs563504489
CDS Mutation c.1289C>T
AA Mutation p.Ser430Leu(p.S430L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000442544
Start 53467994:53467994(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3720C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000442544
Start 53305647:53305647(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1981C>T
AA Mutation p.Arg661Ter(p.R661*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000442544
Start 53499408:53499408(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773315729
CDS Mutation c.4009C>T
AA Mutation p.Arg1337Ter(p.R1337*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000442544
Start 53339814:53339814(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2266C>T
AA Mutation p.Arg756Ter(p.R756*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript