Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TTC28

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27983768:27983768(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5899G>A
AA Mutation p.Ala1967Thr(p.A1967T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28030342:28030342(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3957G>T
AA Mutation p.Glu1319Asp(p.E1319D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28107434:28107434(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2411A>G
AA Mutation p.Tyr804Cys(p.Y804C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28163388:28163388(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1145A>T
AA Mutation p.Lys382Met(p.K382M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28096275:28096275(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3681G>T
AA Mutation p.Glu1227Asp(p.E1227D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27982625:27982625(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs111364834
CDS Mutation c.7042G>A
AA Mutation p.Ala2348Thr(p.A2348T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28107408:28107408(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2437G>A
AA Mutation p.Ala813Thr(p.A813T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27996230:27996230(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5149C>A
AA Mutation p.Leu1717Met(p.L1717M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28098933:28098933(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3529C>T
AA Mutation p.Arg1177Trp(p.R1177W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27983615:27983615(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6052G>A
AA Mutation p.Gly2018Arg(p.G2018R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27983593:27983593(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746058646
CDS Mutation c.6074G>A
AA Mutation p.Arg2025Gln(p.R2025Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27998741:27998741(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4918G>A
AA Mutation p.Ala1640Thr(p.A1640T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28107126:28107126(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772960214
CDS Mutation c.2719G>A
AA Mutation p.Ala907Thr(p.A907T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27998983:27998983(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4676C>T
AA Mutation p.Thr1559Met(p.T1559M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28107125:28107125(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777828084
CDS Mutation c.2720C>T
AA Mutation p.Ala907Val(p.A907V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28107110:28107110(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779754496
CDS Mutation c.2735G>A
AA Mutation p.Arg912His(p.R912H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28163502:28163502(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1031C>T
AA Mutation p.Ala344Val(p.A344V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28014259:28014259(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4207C>G
AA Mutation p.Pro1403Ala(p.P1403A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28296271:28296271(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs181453650
CDS Mutation c.860A>G
AA Mutation p.Lys287Arg(p.K287R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27996236:27996236(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5143G>A
AA Mutation p.Val1715Ile(p.V1715I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27999171:27999171(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4488G>T
AA Mutation p.Met1496Ile(p.M1496I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27996242:27996242(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5137A>G
AA Mutation p.Ser1713Gly(p.S1713G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28108253:28108253(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1592A>G
AA Mutation p.Asp531Gly(p.D531G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000397906
Start 28629552:28629552(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.381G>T
AA Mutation p.Lys127Asn(p.K127N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27993481:27993481(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748910267
CDS Mutation c.5282G>A
AA Mutation p.Arg1761His(p.R1761H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27983116:27983116(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6551G>A
AA Mutation p.Gly2184Asp(p.G2184D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27982364:27982364(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs529389400
CDS Mutation c.7303C>T
AA Mutation p.Arg2435Cys(p.R2435C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28030252:28030252(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4047G>A
AA Mutation p.Met1349Ile(p.M1349I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 28105709:28105709(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765546235
CDS Mutation c.2877C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27998909:27998909(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4750C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 28107682:28107682(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2163C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27983070:27983070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6597G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27993405:27993405(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5358C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 28001422:28001422(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776015784
CDS Mutation c.4350C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27996159:27996159(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs538933416
CDS Mutation c.5220C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27999240:27999240(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4419G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27985261:27985261(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5803C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27983229:27983229(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767347871
CDS Mutation c.6438C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 28107184:28107184(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762688264
CDS Mutation c.2661C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 28107874:28107874(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1971C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 28108162:28108162(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs555749441
CDS Mutation c.1683C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27982647:27982647(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775969352
CDS Mutation c.7020C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27982881:27982881(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs533331940
CDS Mutation c.6786C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 28163114:28163114(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1419G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27982332:27982332(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771522552
CDS Mutation c.7335G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27982707:27982707(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6960C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence frameshift_variant
Transcription ID ENST00000397906
Start 27993379:27993379(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5384delC
AA Mutation p.Pro1795GlnfsTer108(p.P1795Qfs*108)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000397906
Start 28094099:28094099(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3913delG
AA Mutation p.Val1305TrpfsTer29(p.V1305Wfs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000397906
Start 27982526:27982526(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7141delG
AA Mutation p.Ala2381LeufsTer5(p.A2381Lfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 50
Mutation Consequence stop_gained
Transcription ID ENST00000397906
Start 27983453:27983453(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6214G>T
AA Mutation p.Glu2072Ter(p.E2072*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 51
Mutation Consequence stop_gained
Transcription ID ENST00000397906
Start 28107756:28107756(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2089C>T
AA Mutation p.Gln697Ter(p.Q697*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000397906
Start 28306634:28306634(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.391C>T
AA Mutation p.Arg131Ter(p.R131*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence stop_gained
Transcription ID ENST00000397906
Start 28096373:28096373(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3583G>T
AA Mutation p.Gly1195Ter(p.G1195*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence stop_gained
Transcription ID ENST00000397906
Start 27985294:27985294(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5770C>T
AA Mutation p.Arg1924Ter(p.R1924*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 55
Mutation Consequence stop_gained
Transcription ID ENST00000397906
Start 28107877:28107877(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1968C>A
AA Mutation p.Tyr656Ter(p.Y656*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 56
Mutation Consequence frameshift_variant
Transcription ID ENST00000397906
Start 28107660:28107661(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2184dupA
AA Mutation p.Asp729ArgfsTer10(p.D729Rfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TTC28

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27992609:27992609(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5531C>T
AA Mutation p.Thr1844Met(p.T1844M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28108302:28108302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1543C>T
AA Mutation p.Arg515Cys(p.R515C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28107873:28107873(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1972G>A
AA Mutation p.Glu658Lys(p.E658K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27983399:27983399(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6268G>A
AA Mutation p.Ala2090Thr(p.A2090T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 27990805:27990805(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5561A>C
AA Mutation p.Lys1854Thr(p.K1854T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000397906
Start 28629796:28629796(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.137G>T
AA Mutation p.Arg46Ile(p.R46I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27982299:27982299(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757345038
CDS Mutation c.7368G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27982239:27982239(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7428C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27982359:27982359(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766284253
CDS Mutation c.7308C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 28030282:28030282(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745548425
CDS Mutation c.4017G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 27999114:27999114(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4545C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 28001449:28001449(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4323C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000397906
Start 28030288:28030288(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4011C>A
Mutation Classification Silent
Feature Type Transcript