Primary Site >> Stomach Cancer
Gene >> TRIOBP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37735423:37735423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5087C>A |
| AA Mutation | p.Pro1696His(p.P1696H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37734544:37734544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4208C>T |
| AA Mutation | p.Pro1403Leu(p.P1403L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37755596:37755596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752167697 |
| CDS Mutation | c.5624G>A |
| AA Mutation | p.Arg1875Gln(p.R1875Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37715788:37715788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.482A>C |
| AA Mutation | p.Glu161Ala(p.E161A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37759256:37759256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6316A>T |
| AA Mutation | p.Ile2106Phe(p.I2106F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37715878:37715878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201532915 |
| CDS Mutation | c.572C>T |
| AA Mutation | p.Pro191Leu(p.P191L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37724620:37724620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2064C>A |
| AA Mutation | p.Ser688Arg(p.S688R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37723853:37723853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551767434 |
| CDS Mutation | c.1297G>A |
| AA Mutation | p.Ala433Thr(p.A433T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37701430:37701430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761159399 |
| CDS Mutation | c.65G>A |
| AA Mutation | p.Arg22His(p.R22H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37725368:37725368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753851434 |
| CDS Mutation | c.2812G>A |
| AA Mutation | p.Ala938Thr(p.A938T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37734879:37734879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543930307 |
| CDS Mutation | c.4543C>T |
| AA Mutation | p.Pro1515Ser(p.P1515S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37758101:37758101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6176G>T |
| AA Mutation | p.Gly2059Val(p.G2059V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37715810:37715810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs116448422 |
| CDS Mutation | c.504C>G |
| AA Mutation | p.Asp168Glu(p.D168E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37724525:37724525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770347004 |
| CDS Mutation | c.1969G>A |
| AA Mutation | p.Asp657Asn(p.D657N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37725813:37725813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3257C>A |
| AA Mutation | p.Pro1086His(p.P1086H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37734963:37734963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4627G>C |
| AA Mutation | p.Gly1543Arg(p.G1543R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37724826:37724826(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2270C>A |
| AA Mutation | p.Ser757Tyr(p.S757Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37734626:37734626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4290G>T |
| AA Mutation | p.Gln1430His(p.Q1430H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37723506:37723506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.950A>T |
| AA Mutation | p.Glu317Val(p.E317V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37769105:37769105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6653C>T |
| AA Mutation | p.Ala2218Val(p.A2218V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37723692:37723692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1136G>A |
| AA Mutation | p.Arg379Lys(p.R379K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37755144:37755144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5531A>G |
| AA Mutation | p.Asp1844Gly(p.D1844G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406386 |
| Start | 37755108:37755108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5495A>T |
| AA Mutation | p.Glu1832Val(p.E1832V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406386 |
| Start | 37723555:37723555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.999A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406386 |
| Start | 37724698:37724698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2142C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406386 |
| Start | 37725661:37725661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571174817 |
| CDS Mutation | c.3105C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406386 |
| Start | 37734968:37734968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765744248 |
| CDS Mutation | c.4632G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406386 |
| Start | 37726357:37726357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3801G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406386 |
| Start | 37724842:37724842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2286C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406386 |
| Start | 37758003:37758003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6078C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406386 |
| Start | 37726162:37726162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3606C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000406386 |
| Start | 37725794:37725794(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3238delA |
| AA Mutation | p.Thr1080ProfsTer133(p.T1080Pfs*133) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 33 |
| 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 |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000406386 |
| Start | 37734519:37734519(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4188delC |
| AA Mutation | p.Arg1397GlyfsTer47(p.R1397Gfs*47) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000406386 |
| Start | 37723542:37723542(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.990delC |
| AA Mutation | p.Arg331GlyfsTer548(p.R331Gfs*548) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000406386 |
| Start | 37725765:37725765(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3214delC |
| AA Mutation | p.Arg1072GlyfsTer141(p.R1072Gfs*141) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000406386 |
| Start | 37725328:37725328(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2772delA |
| AA Mutation | p.Ser925LeufsTer80(p.S925Lfs*80) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000406386 |
| Start | 37734716:37734716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776530766 |
| CDS Mutation | c.4380G>A |
| AA Mutation | p.Trp1460Ter(p.W1460*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000406386 |
| Start | 37724777:37724777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546890298 |
| CDS Mutation | c.2221C>T |
| AA Mutation | p.Arg741Ter(p.R741*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000406386 |
| Start | 37769155:37769155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6703C>T |
| AA Mutation | p.Gln2235Ter(p.Q2235*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000406386 |
| Start | 37724417:37724417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747160833 |
| CDS Mutation | c.1861C>T |
| AA Mutation | p.Arg621Ter(p.R621*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| 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 |
| ID | 43 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000406386 |
| Start | 37725821:37725822(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3268_3273dupGACACA |
| AA Mutation | p.Asp1090_Thr1091dup(p.D1090_T1091dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |