Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNS1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818706:217818706(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150702291
CDS Mutation c.3314C>T
AA Mutation p.Thr1105Met(p.T1105M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217848299:217848299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1843G>A
AA Mutation p.Gly615Ser(p.G615S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217885752:217885752(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.733G>T
AA Mutation p.Asp245Tyr(p.D245Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818649:217818649(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3371G>A
AA Mutation p.Ser1124Asn(p.S1124N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217880949:217880949(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1003C>T
AA Mutation p.Arg335Cys(p.R335C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217848387:217848387(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1755G>T
AA Mutation p.Gln585His(p.Q585H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818748:217818748(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3272G>T
AA Mutation p.Gly1091Val(p.G1091V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217804587:217804587(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5080G>A
AA Mutation p.Ala1694Thr(p.A1694T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217848604:217848604(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs116507626
CDS Mutation c.1538C>T
AA Mutation p.Ala513Val(p.A513V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217897959:217897959(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7G>A
AA Mutation p.Val3Met(p.V3M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818379:217818379(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3641A>G
AA Mutation p.His1214Arg(p.H1214R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217848745:217848745(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368810573
CDS Mutation c.1397G>A
AA Mutation p.Arg466His(p.R466H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217848392:217848392(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1750G>A
AA Mutation p.Ala584Thr(p.A584T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217848776:217848776(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770522095
CDS Mutation c.1366G>A
AA Mutation p.Ala456Thr(p.A456T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217813245:217813245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4612C>T
AA Mutation p.Leu1538Phe(p.L1538F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217885769:217885769(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.716G>A
AA Mutation p.Gly239Glu(p.G239E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818195:217818195(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3825C>A
AA Mutation p.His1275Gln(p.H1275Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217886561:217886561(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs576154784
CDS Mutation c.577G>A
AA Mutation p.Gly193Ser(p.G193S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217848487:217848487(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1655C>T
AA Mutation p.Pro552Leu(p.P552L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217836103:217836103(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs186255060
CDS Mutation c.2741G>A
AA Mutation p.Arg914His(p.R914H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818040:217818040(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3980C>G
AA Mutation p.Ser1327Cys(p.S1327C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217810316:217810316(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4724C>A
AA Mutation p.Pro1575His(p.P1575H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818502:217818502(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138956630
CDS Mutation c.3518C>T
AA Mutation p.Thr1173Met(p.T1173M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818064:217818064(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375150652
CDS Mutation c.3956G>A
AA Mutation p.Arg1319Gln(p.R1319Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217831481:217831481(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139665137
CDS Mutation c.2972C>T
AA Mutation p.Ala991Val(p.A991V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217809875:217809875(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201730716
CDS Mutation c.4909G>A
AA Mutation p.Val1637Ile(p.V1637I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217890965:217890965(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.488G>T
AA Mutation p.Arg163Ile(p.R163I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217893005:217893005(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750425819
CDS Mutation c.350G>A
AA Mutation p.Arg117Gln(p.R117Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217847858:217847858(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2284T>C
AA Mutation p.Ser762Pro(p.S762P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217848014:217848014(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200562336
CDS Mutation c.2128G>A
AA Mutation p.Glu710Lys(p.E710K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818107:217818107(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202059695
CDS Mutation c.3913G>A
AA Mutation p.Gly1305Arg(p.G1305R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818634:217818634(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3386G>T
AA Mutation p.Arg1129Ile(p.R1129I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818110:217818110(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3910C>A
AA Mutation p.Leu1304Ile(p.L1304I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217818056:217818056(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3964G>A
AA Mutation p.Ala1322Thr(p.A1322T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217821770:217821770(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3230C>A
AA Mutation p.Ser1077Tyr(p.S1077Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217818546:217818546(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760755214
CDS Mutation c.3474G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217813809:217813809(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768725508
CDS Mutation c.4425G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217813240:217813240(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4617G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217818081:217818081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3939C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217821838:217821838(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3162C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217835095:217835095(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748677064
CDS Mutation c.2901T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217813788:217813788(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4446G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217810252:217810252(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4788G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217818054:217818054(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3966C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217885777:217885777(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 ENST00000171887
Start 217818477:217818477(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3543C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000171887
Start 217831535:217831535(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2918delC
AA Mutation p.Pro973ArgfsTer13(p.P973Rfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000171887
Start 217848232:217848232(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1910delG
AA Mutation p.Gly637GlufsTer11(p.G637Efs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000171887
Start 217848733:217848733(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1409delG
AA Mutation p.Gly470AlafsTer23(p.G470Afs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000171887
Start 217848547:217848547(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1595delG
AA Mutation p.Gly532AlafsTer9(p.G532Afs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 51
Mutation Consequence stop_gained
Transcription ID ENST00000171887
Start 217885128:217885128(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.778C>T
AA Mutation p.Arg260Ter(p.R260*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence splice_donor_variant
Transcription ID ENST00000171887
Start 217817688:217817688(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4330+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 53
Mutation Consequence splice_donor_variant
Transcription ID ENST00000171887
Start 217813213:217813213(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4642+2T>C
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> TNS1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217885776:217885776(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370385101
CDS Mutation c.709G>A
AA Mutation p.Glu237Lys(p.E237K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217848274:217848274(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751419226
CDS Mutation c.1868C>T
AA Mutation p.Ser623Leu(p.S623L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217847533:217847533(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2609G>A
AA Mutation p.Gly870Glu(p.G870E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217814928:217814928(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4401G>T
AA Mutation p.Glu1467Asp(p.E1467D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000171887
Start 217880934:217880934(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1018G>A
AA Mutation p.Asp340Asn(p.D340N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217848729:217848729(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758569137
CDS Mutation c.1413G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217848966:217848966(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1176C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217849035:217849035(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1107G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217810303:217810303(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201334905
CDS Mutation c.4737G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217817910:217817910(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758537443
CDS Mutation c.4110G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000171887
Start 217895021:217895021(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750884795
CDS Mutation c.204G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence inframe_deletion
Transcription ID ENST00000171887
Start 217814949:217814951(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4378_4380delTCT
AA Mutation p.Ser1460del(p.S1460del)
Mutation Classification In_Frame_Del
Feature Type Transcript