Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TDRD6

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46692063:46692063(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3935C>A
AA Mutation p.Ser1312Tyr(p.S1312Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46690388:46690388(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2260A>T
AA Mutation p.Asn754Tyr(p.N754Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46693224:46693224(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5096C>A
AA Mutation p.Ser1699Tyr(p.S1699Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46693899:46693899(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5771C>A
AA Mutation p.Ser1924Tyr(p.S1924Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46691327:46691327(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3199T>G
AA Mutation p.Phe1067Val(p.F1067V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46691317:46691317(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3189C>A
AA Mutation p.Phe1063Leu(p.F1063L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46691752:46691752(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3624T>G
AA Mutation p.Ile1208Met(p.I1208M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46691805:46691805(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3677T>C
AA Mutation p.Leu1226Pro(p.L1226P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46692332:46692332(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4204G>T
AA Mutation p.Gly1402Cys(p.G1402C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46688846:46688846(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.718G>T
AA Mutation p.Asp240Tyr(p.D240Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46688916:46688916(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.788A>G
AA Mutation p.His263Arg(p.H263R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46689231:46689231(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373561239
CDS Mutation c.1103G>A
AA Mutation p.Arg368Gln(p.R368Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46689134:46689134(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746421668
CDS Mutation c.1006C>T
AA Mutation p.Arg336Trp(p.R336W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46693245:46693245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5117C>T
AA Mutation p.Ala1706Val(p.A1706V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46695934:46695934(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6160G>A
AA Mutation p.Glu2054Lys(p.E2054K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46688912:46688912(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.784C>T
AA Mutation p.Pro262Ser(p.P262S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46691990:46691990(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3862G>T
AA Mutation p.Asp1288Tyr(p.D1288Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46690571:46690571(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772802461
CDS Mutation c.2443C>T
AA Mutation p.Pro815Ser(p.P815S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46691443:46691443(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3315T>G
AA Mutation p.Asp1105Glu(p.D1105E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46692659:46692659(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4531C>A
AA Mutation p.Leu1511Ile(p.L1511I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46692984:46692984(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4856C>T
AA Mutation p.Ala1619Val(p.A1619V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46693559:46693559(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5431T>C
AA Mutation p.Tyr1811His(p.Y1811H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46693032:46693032(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4904G>T
AA Mutation p.Cys1635Phe(p.C1635F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000316081
Start 46691308:46691308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3180G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000316081
Start 46691797:46691797(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3669A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000316081
Start 46689331:46689331(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1203A>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000316081
Start 46689721:46689721(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1593T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000316081
Start 46692208:46692208(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4080T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000316081
Start 46692283:46692283(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4155G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence frameshift_variant
Transcription ID ENST00000316081
Start 46690872:46690872(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2750delA
AA Mutation p.Asn917IlefsTer2(p.N917Ifs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 31
Mutation Consequence stop_gained
Transcription ID ENST00000316081
Start 46689230:46689230(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1102C>T
AA Mutation p.Arg368Ter(p.R368*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000316081
Start 46691255:46691255(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3127A>T
AA Mutation p.Lys1043Ter(p.K1043*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000316081
Start 46689616:46689617(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1493dupA
AA Mutation p.Asn498LysfsTer4(p.N498Kfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000316081
Start 46689446:46689447(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1319dupG
AA Mutation p.Cys440TrpfsTer5(p.C440Wfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 35
Mutation Consequence frameshift_variant
Transcription ID ENST00000316081
Start 46693034:46693035(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4906_4907insAAAG
AA Mutation p.Leu1636GlnfsTer6(p.L1636Qfs*6)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TDRD6

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46694094:46694094(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150855637
CDS Mutation c.5966C>T
AA Mutation p.Ser1989Leu(p.S1989L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46693352:46693352(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5224T>A
AA Mutation p.Tyr1742Asn(p.Y1742N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46690950:46690950(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2822T>C
AA Mutation p.Leu941Pro(p.L941P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46701863:46701863(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6267G>C
AA Mutation p.Arg2089Ser(p.R2089S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46695878:46695878(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6104T>G
AA Mutation p.Val2035Gly(p.V2035G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46690206:46690206(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756938796
CDS Mutation c.2078C>T
AA Mutation p.Thr693Met(p.T693M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46690562:46690562(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2434A>G
AA Mutation p.Thr812Ala(p.T812A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000316081
Start 46693128:46693128(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5000T>G
AA Mutation p.Ile1667Arg(p.I1667R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000316081
Start 46690027:46690027(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1899T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000316081
Start 46689230:46689230(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1102C>T
AA Mutation p.Arg368Ter(p.R368*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000316081
Start 46690871:46690872(version: GRCh38)
Mutation Type INS
dbSNP_RS rs765467808
CDS Mutation c.2750dupA
AA Mutation p.Asn917LysfsTer15(p.N917Kfs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript