Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DAPK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87642008:87642008(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.868G>C
AA Mutation p.Ala290Pro(p.A290P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87640371:87640371(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs548113187
CDS Mutation c.703G>A
AA Mutation p.Glu235Lys(p.E235K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87650065:87650065(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776122467
CDS Mutation c.1573G>A
AA Mutation p.Asp525Asn(p.D525N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87706489:87706489(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3418T>C
AA Mutation p.Phe1140Leu(p.F1140L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87668670:87668670(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369031259
CDS Mutation c.1997G>A
AA Mutation p.Arg666Gln(p.R666Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87681485:87681485(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2083C>T
AA Mutation p.His695Tyr(p.H695Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87681561:87681561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2159G>A
AA Mutation p.Arg720Gln(p.R720Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87639391:87639391(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.461A>C
AA Mutation p.Lys154Thr(p.K154T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87605064:87605064(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375169492
CDS Mutation c.173G>A
AA Mutation p.Arg58His(p.R58H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87706412:87706412(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375598719
CDS Mutation c.3341G>A
AA Mutation p.Arg1114His(p.R1114H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87706435:87706435(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3364G>A
AA Mutation p.Glu1122Lys(p.E1122K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87703207:87703207(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3050G>A
AA Mutation p.Ser1017Asn(p.S1017N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87706918:87706918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3847A>G
AA Mutation p.Met1283Val(p.M1283V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87686592:87686592(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2266G>A
AA Mutation p.Val756Met(p.V756M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87707298:87707298(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4227G>T
AA Mutation p.Glu1409Asp(p.E1409D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87605048:87605048(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774238093
CDS Mutation c.157C>T
AA Mutation p.Arg53Trp(p.R53W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87649972:87649972(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1480G>A
AA Mutation p.Ala494Thr(p.A494T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87700136:87700136(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2770A>T
AA Mutation p.Ile924Phe(p.I924F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87604983:87604983(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777469310
CDS Mutation c.92G>A
AA Mutation p.Arg31His(p.R31H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87648827:87648827(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1376A>C
AA Mutation p.Asp459Ala(p.D459A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87700200:87700200(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748494486
CDS Mutation c.2834G>A
AA Mutation p.Arg945Gln(p.R945Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87651530:87651530(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200262418
CDS Mutation c.1630G>A
AA Mutation p.Gly544Arg(p.G544R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87706324:87706324(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3253C>A
AA Mutation p.Leu1085Ile(p.L1085I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87640308:87640308(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749825789
CDS Mutation c.640G>A
AA Mutation p.Ala214Thr(p.A214T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87706846:87706846(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771500801
CDS Mutation c.3775C>T
AA Mutation p.Arg1259Trp(p.R1259W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87697031:87697031(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2438A>C
AA Mutation p.Glu813Ala(p.E813A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87706164:87706164(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371818389
CDS Mutation c.3093C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87649992:87649992(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765826018
CDS Mutation c.1500C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87650085:87650085(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773562327
CDS Mutation c.1593C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87706935:87706935(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201377316
CDS Mutation c.3864C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87649936:87649936(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1444C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87650034:87650034(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1542C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87605065:87605065(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200958656
CDS Mutation c.174C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87681601:87681601(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2199T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87706434:87706434(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769931498
CDS Mutation c.3363C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87650017:87650017(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1525C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87651607:87651607(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755628476
CDS Mutation c.1707C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87706560:87706560(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768494372
CDS Mutation c.3489C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87706749:87706749(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202069940
CDS Mutation c.3678G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87647349:87647349(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs55637131
CDS Mutation c.1275C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87697032:87697032(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2439G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87686678:87686678(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750748509
CDS Mutation c.2352G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence frameshift_variant
Transcription ID ENST00000358077
Start 87706887:87706887(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3822delG
AA Mutation p.Tyr1275ThrfsTer31(p.Y1275Tfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000358077
Start 87681500:87681500(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2101delA
AA Mutation p.Thr701ProfsTer4(p.T701Pfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000358077
Start 87642047:87642047(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.912delA
AA Mutation p.Lys304AsnfsTer8(p.K304Nfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 46
Mutation Consequence stop_gained
Transcription ID ENST00000358077
Start 87700220:87700220(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749723265
CDS Mutation c.2854C>T
AA Mutation p.Arg952Ter(p.R952*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000358077
Start 87637984:87637985(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.326_327insTT
AA Mutation p.Glu109AspfsTer4(p.E109Dfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> DAPK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87646537:87646537(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1208C>T
AA Mutation p.Ser403Leu(p.S403L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000358077
Start 87639483:87639483(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761997264
CDS Mutation c.553G>A
AA Mutation p.Ala185Thr(p.A185T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87647363:87647363(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1289T>A
AA Mutation p.Phe430Tyr(p.F430Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000358077
Start 87706471:87706471(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3400G>C
AA Mutation p.Val1134Leu(p.V1134L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87706911:87706911(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3840C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87605131:87605131(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs36207429
CDS Mutation c.240C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87686627:87686627(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371530974
CDS Mutation c.2301G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000358077
Start 87707115:87707115(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4044G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000358077
Start 87700199:87700199(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2833C>T
AA Mutation p.Arg945Ter(p.R945*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript