Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRIOBP

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37723265:37723265(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144995033
CDS Mutation c.709C>T
AA Mutation p.Arg237Trp(p.R237W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37765701:37765701(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6356A>T
AA Mutation p.Glu2119Val(p.E2119V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37724759:37724759(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758476559
CDS Mutation c.2203C>T
AA Mutation p.Arg735Cys(p.R735C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37771683:37771683(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6883T>C
AA Mutation p.Tyr2295His(p.Y2295H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37726331:37726331(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755555403
CDS Mutation c.3775G>A
AA Mutation p.Gly1259Arg(p.G1259R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37723551:37723551(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.995C>T
AA Mutation p.Ala332Val(p.A332V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37735290:37735290(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4954G>T
AA Mutation p.Val1652Phe(p.V1652F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37724921:37724921(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2365G>T
AA Mutation p.Asp789Tyr(p.D789Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37723190:37723190(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201794404
CDS Mutation c.634G>A
AA Mutation p.Gly212Ser(p.G212S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37725795:37725795(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766097053
CDS Mutation c.3239C>T
AA Mutation p.Thr1080Ile(p.T1080I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37725918:37725918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3362G>A
AA Mutation p.Arg1121Gln(p.R1121Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37740995:37740995(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374789338
CDS Mutation c.5285C>T
AA Mutation p.Pro1762Leu(p.P1762L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37725789:37725789(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199940075
CDS Mutation c.3233G>A
AA Mutation p.Arg1078His(p.R1078H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37757798:37757798(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5873G>A
AA Mutation p.Arg1958Gln(p.R1958Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37759248:37759248(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200250028
CDS Mutation c.6308C>T
AA Mutation p.Pro2103Leu(p.P2103L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37772674:37772674(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200850285
CDS Mutation c.7010G>A
AA Mutation p.Arg2337Gln(p.R2337Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37740953:37740953(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5243C>T
AA Mutation p.Thr1748Ile(p.T1748I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37757689:37757689(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs183941928
CDS Mutation c.5764C>T
AA Mutation p.Arg1922Trp(p.R1922W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37758056:37758056(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6131T>C
AA Mutation p.Val2044Ala(p.V2044A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37734488:37734488(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4152G>T
AA Mutation p.Glu1384Asp(p.E1384D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37701459:37701459(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.94G>C
AA Mutation p.Ala32Pro(p.A32P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37723797:37723797(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1241C>A
AA Mutation p.Ala414Asp(p.A414D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37724846:37724846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2290C>A
AA Mutation p.Gln764Lys(p.Q764K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37725030:37725030(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2474G>A
AA Mutation p.Arg825Lys(p.R825K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37757723:37757723(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5798C>A
AA Mutation p.Pro1933His(p.P1933H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37755595:37755595(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778674956
CDS Mutation c.5623C>T
AA Mutation p.Arg1875Trp(p.R1875W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37724664:37724664(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779032542
CDS Mutation c.2108G>A
AA Mutation p.Arg703Gln(p.R703Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37725453:37725453(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2897G>T
AA Mutation p.Gly966Val(p.G966V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37735387:37735387(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375129555
CDS Mutation c.5051C>T
AA Mutation p.Thr1684Met(p.T1684M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000406386
Start 37715849:37715849(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.543G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000406386
Start 37771673:37771673(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768762605
CDS Mutation c.6873C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000406386
Start 37740972:37740972(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5262G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000406386
Start 37724869:37724869(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2313C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000406386
Start 37725325:37725325(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2769C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence frameshift_variant
Transcription ID ENST00000406386
Start 37734766:37734766(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs778824544
CDS Mutation c.4436delG
AA Mutation p.Gly1479AlafsTer28(p.G1479Afs*28)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000406386
Start 37723530:37723530(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.976delC
AA Mutation p.Gln326LysfsTer553(p.Q326Kfs*553)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 37
Mutation Consequence frameshift_variant
Transcription ID ENST00000406386
Start 37713257:37713257(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.306delC
AA Mutation p.Arg103GlyfsTer16(p.R103Gfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 38
Mutation Consequence frameshift_variant
Transcription ID ENST00000406386
Start 37725855:37725855(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3304delC
AA Mutation p.Gln1102AsnfsTer111(p.Q1102Nfs*111)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 39
Mutation Consequence stop_gained
Transcription ID ENST00000406386
Start 37734849:37734849(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4513G>T
AA Mutation p.Glu1505Ter(p.E1505*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence frameshift_variant
Transcription ID ENST00000406386
Start 37765698:37765699(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.6355dupG
AA Mutation p.Glu2119GlyfsTer32(p.E2119Gfs*32)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 41
Mutation Consequence frameshift_variant
Transcription ID ENST00000406386
Start 37734877:37734878(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4547dupC
AA Mutation p.Glu1517Ter(p.E1517*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 42
Mutation Consequence frameshift_variant
Transcription ID ENST00000406386
Start 37741018:37741019(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.5308_5309insAGTGT
AA Mutation p.Leu1770GlnfsTer47(p.L1770Qfs*47)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TRIOBP

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37734814:37734814(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4478C>T
AA Mutation p.Ala1493Val(p.A1493V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37725761:37725761(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3205G>T
AA Mutation p.Asp1069Tyr(p.D1069Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37754911:37754911(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758269503
CDS Mutation c.5414C>T
AA Mutation p.Ser1805Leu(p.S1805L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37723620:37723620(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1064G>T
AA Mutation p.Arg355Ile(p.R355I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37725525:37725525(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758243873
CDS Mutation c.2969G>A
AA Mutation p.Arg990Gln(p.R990Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000406386
Start 37735188:37735188(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4852A>G
AA Mutation p.Thr1618Ala(p.T1618A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000406386
Start 37713258:37713258(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.303C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000406386
Start 37734996:37734996(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4660C>T
AA Mutation p.Arg1554Ter(p.R1554*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript