Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRRAP

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98977014:98977014(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371221629
CDS Mutation c.8302C>T
AA Mutation p.Arg2768Trp(p.R2768W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98988874:98988874(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778465879
CDS Mutation c.9511C>T
AA Mutation p.Arg3171Trp(p.R3171W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000359863
Start 98930634:98930634(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3395C>T
AA Mutation p.Ala1132Val(p.A1132V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98994823:98994823(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10242G>T
AA Mutation p.Gln3414His(p.Q3414H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 99012296:99012296(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759268268
CDS Mutation c.11521G>A
AA Mutation p.Ala3841Thr(p.A3841T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98965764:98965764(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7024A>G
AA Mutation p.Met2342Val(p.M2342V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98915841:98915841(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2318A>C
AA Mutation p.Asp773Ala(p.D773A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98953321:98953321(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5597G>T
AA Mutation p.Trp1866Leu(p.W1866L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98948609:98948609(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4691G>A
AA Mutation p.Arg1564Gln(p.R1564Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98981916:98981916(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8761C>T
AA Mutation p.Arg2921Trp(p.R2921W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98935646:98935646(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4082C>T
AA Mutation p.Ser1361Leu(p.S1361L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98990509:98990509(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9658G>A
AA Mutation p.Asp3220Asn(p.D3220N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98897816:98897816(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.583A>G
AA Mutation p.Thr195Ala(p.T195A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98892459:98892459(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.297A>T
AA Mutation p.Arg99Ser(p.R99S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98953428:98953428(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5704C>A
AA Mutation p.Leu1902Met(p.L1902M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98925167:98925167(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2879G>A
AA Mutation p.Arg960Gln(p.R960Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98978314:98978314(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8468A>G
AA Mutation p.His2823Arg(p.H2823R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 99011155:99011155(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145586252
CDS Mutation c.11000C>T
AA Mutation p.Thr3667Met(p.T3667M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98908951:98908951(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782078583
CDS Mutation c.1339C>T
AA Mutation p.Arg447Trp(p.R447W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98953425:98953425(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5701G>A
AA Mutation p.Val1901Ile(p.V1901I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98948647:98948647(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4729G>A
AA Mutation p.Ala1577Thr(p.A1577T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98993627:98993627(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9895C>T
AA Mutation p.Arg3299Cys(p.R3299C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98933318:98933318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3930G>T
AA Mutation p.Glu1310Asp(p.E1310D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98949528:98949528(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782510081
CDS Mutation c.4879G>A
AA Mutation p.Gly1627Ser(p.G1627S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 99008455:99008455(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10790A>G
AA Mutation p.Tyr3597Cys(p.Y3597C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98953347:98953347(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5623G>A
AA Mutation p.Val1875Met(p.V1875M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98981947:98981947(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8792C>T
AA Mutation p.Thr2931Met(p.T2931M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98965767:98965767(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7027C>T
AA Mutation p.Arg2343Trp(p.R2343W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98911259:98911259(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1995T>A
AA Mutation p.Asn665Lys(p.N665K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98956513:98956513(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6190G>A
AA Mutation p.Ala2064Thr(p.A2064T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98930720:98930720(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3481G>A
AA Mutation p.Val1161Met(p.V1161M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98942959:98942959(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4415G>A
AA Mutation p.Arg1472His(p.R1472H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98984332:98984332(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200203849
CDS Mutation c.9274G>A
AA Mutation p.Val3092Ile(p.V3092I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98933298:98933298(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3910G>A
AA Mutation p.Ala1304Thr(p.A1304T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98948318:98948318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4625C>T
AA Mutation p.Thr1542Met(p.T1542M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98978864:98978864(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8573G>A
AA Mutation p.Arg2858Gln(p.R2858Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98931459:98931459(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757085445
CDS Mutation c.3646C>T
AA Mutation p.Arg1216Trp(p.R1216W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98950198:98950198(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5249G>A
AA Mutation p.Arg1750His(p.R1750H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98983309:98983309(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs537483764
CDS Mutation c.8851G>A
AA Mutation p.Ala2951Thr(p.A2951T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98900656:98900656(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.833C>T
AA Mutation p.Ala278Val(p.A278V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98930645:98930645(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3406C>T
AA Mutation p.Pro1136Ser(p.P1136S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98984971:98984971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9328T>G
AA Mutation p.Leu3110Val(p.L3110V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98970172:98970172(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764666499
CDS Mutation c.7552C>T
AA Mutation p.Leu2518Phe(p.L2518F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98967646:98967646(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7439C>T
AA Mutation p.Ser2480Leu(p.S2480L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98949454:98949454(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4805A>G
AA Mutation p.Asp1602Gly(p.D1602G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 46
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98953336:98953336(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5612C>G
AA Mutation p.Ser1871Cys(p.S1871C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 47
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98964728:98964728(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6908A>G
AA Mutation p.Glu2303Gly(p.E2303G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98961324:98961324(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6532C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 99012259:99012259(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200231900
CDS Mutation c.11484C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98971846:98971846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7719G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98958079:98958079(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782000637
CDS Mutation c.6309C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98976590:98976590(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140761278
CDS Mutation c.8046C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98948319:98948319(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781933256
CDS Mutation c.4626G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98981927:98981927(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753623703
CDS Mutation c.8772C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98955154:98955154(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5766G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98935647:98935647(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782593506
CDS Mutation c.4083A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98971846:98971846(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7719G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98967518:98967518(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs543446866
CDS Mutation c.7311G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 59
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98953235:98953235(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781886929
CDS Mutation c.5511G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 60
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98965739:98965739(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6999G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 61
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98965868:98965868(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7128G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 62
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 99011481:99011481(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140449855
CDS Mutation c.11241G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 63
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98950241:98950241(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782207219
CDS Mutation c.5292C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 64
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98917598:98917598(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2541G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 65
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98948328:98948328(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142246393
CDS Mutation c.4635G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 66
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98943008:98943008(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4464C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 67
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98976959:98976959(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759369634
CDS Mutation c.8247G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 68
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 99011096:99011096(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201702554
CDS Mutation c.10941G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 69
Mutation Consequence frameshift_variant
Transcription ID ENST00000359863
Start 98900691:98900691(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.872delT
AA Mutation p.Leu291Ter(p.L291*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 70
Mutation Consequence frameshift_variant
Transcription ID ENST00000359863
Start 99004246:99004246(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.10328delA
AA Mutation p.Lys3443SerfsTer19(p.K3443Sfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 71
Mutation Consequence frameshift_variant
Transcription ID ENST00000359863
Start 98933258:98933258(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3875delC
AA Mutation p.Pro1292LeufsTer17(p.P1292Lfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 72
Mutation Consequence stop_gained
Transcription ID ENST00000359863
Start 98949729:98949729(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5002C>T
AA Mutation p.Arg1668Ter(p.R1668*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 73
Mutation Consequence stop_gained
Transcription ID ENST00000359863
Start 99011371:99011371(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11131C>T
AA Mutation p.Arg3711Ter(p.R3711*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 74
Mutation Consequence stop_gained
Transcription ID ENST00000359863
Start 98953245:98953245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5521G>T
AA Mutation p.Glu1841Ter(p.E1841*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 75
Mutation Consequence frameshift_variant
Transcription ID ENST00000359863
Start 98949499:98949500(version: GRCh38)
Mutation Type INS
dbSNP_RS rs781980072
CDS Mutation c.4856dupG
AA Mutation p.Ala1620CysfsTer35(p.A1620Cfs*35)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 76
Mutation Consequence frameshift_variant
Transcription ID ENST00000359863
Start 98935641:98935642(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4077_4078insGCAAATAA
AA Mutation p.Pro1360AlafsTer14(p.P1360Afs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 77
Mutation Consequence frameshift_variant
Transcription ID ENST00000359863
Start 98910389:98910390(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1688dupG
AA Mutation p.Ile564HisfsTer9(p.I564Hfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TRRAP

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98911176:98911176(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1912G>C
AA Mutation p.Val638Leu(p.V638L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98977027:98977027(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770812441
CDS Mutation c.8315C>T
AA Mutation p.Ser2772Leu(p.S2772L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98955174:98955174(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5786C>T
AA Mutation p.Pro1929Leu(p.P1929L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98965833:98965833(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775214250
CDS Mutation c.7093C>T
AA Mutation p.Arg2365Trp(p.R2365W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98967507:98967507(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7300G>A
AA Mutation p.Glu2434Lys(p.E2434K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98892509:98892509(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.347T>C
AA Mutation p.Val116Ala(p.V116A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98897862:98897862(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.629G>A
AA Mutation p.Arg210Gln(p.R210Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98978863:98978863(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8572C>T
AA Mutation p.Arg2858Trp(p.R2858W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98967517:98967517(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774168977
CDS Mutation c.7310C>T
AA Mutation p.Ala2437Val(p.A2437V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000359863
Start 98971863:98971863(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7736T>G
AA Mutation p.Leu2579Arg(p.L2579R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98994634:98994634(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761352412
CDS Mutation c.10053G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98948658:98948658(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144435212
CDS Mutation c.4740C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98965739:98965739(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6999G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 98950890:98950890(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5328C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 99004263:99004263(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10341C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000359863
Start 99011249:99011249(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.11094C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000359863
Start 98925179:98925179(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2891G>A
AA Mutation p.Trp964Ter(p.W964*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000359863
Start 98978322:98978322(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8476C>T
AA Mutation p.Arg2826Ter(p.R2826*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript