Primary Site >> Stomach Cancer
Gene >> TIAM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31182621:31182621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2687T>C |
| AA Mutation | p.Leu896Pro(p.L896P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31266882:31266882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201316248 |
| CDS Mutation | c.91C>T |
| AA Mutation | p.Arg31Cys(p.R31C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31266676:31266676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.297A>C |
| AA Mutation | p.Arg99Ser(p.R99S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31225884:31225884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1651G>A |
| AA Mutation | p.Ala551Thr(p.A551T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31217638:31217638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539113277 |
| CDS Mutation | c.2057C>T |
| AA Mutation | p.Ala686Val(p.A686V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31187012:31187012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2651C>A |
| AA Mutation | p.Ala884Asp(p.A884D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31210092:31210092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775775144 |
| CDS Mutation | c.2341G>A |
| AA Mutation | p.Val781Ile(p.V781I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31141367:31141367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529598323 |
| CDS Mutation | c.3613G>A |
| AA Mutation | p.Ala1205Thr(p.A1205T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31146916:31146916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3454G>T |
| AA Mutation | p.Val1152Phe(p.V1152F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31187042:31187042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2621A>G |
| AA Mutation | p.Tyr874Cys(p.Y874C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31154260:31154260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777057988 |
| CDS Mutation | c.3158G>A |
| AA Mutation | p.Arg1053His(p.R1053H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31217663:31217663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2032C>T |
| AA Mutation | p.Arg678Cys(p.R678C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31266929:31266929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.44G>T |
| AA Mutation | p.Gly15Val(p.G15V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31245657:31245657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1415G>A |
| AA Mutation | p.Cys472Tyr(p.C472Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31120754:31120754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754307192 |
| CDS Mutation | c.4390G>A |
| AA Mutation | p.Ala1464Thr(p.A1464T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31120525:31120525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751890515 |
| CDS Mutation | c.4619G>A |
| AA Mutation | p.Arg1540Gln(p.R1540Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31251958:31251958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1195G>A |
| AA Mutation | p.Glu399Lys(p.E399K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31152745:31152745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3257G>T |
| AA Mutation | p.Gly1086Val(p.G1086V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31120712:31120712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772268816 |
| CDS Mutation | c.4432G>A |
| AA Mutation | p.Gly1478Arg(p.G1478R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31120531:31120531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4613G>A |
| AA Mutation | p.Arg1538Lys(p.R1538K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31202945:31202945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2456T>G |
| AA Mutation | p.Leu819Arg(p.L819R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31154293:31154293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767409099 |
| CDS Mutation | c.3125G>A |
| AA Mutation | p.Arg1042His(p.R1042H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31120789:31120789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4355G>A |
| AA Mutation | p.Arg1452Gln(p.R1452Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31130216:31130216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769275298 |
| CDS Mutation | c.4042G>A |
| AA Mutation | p.Ala1348Thr(p.A1348T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31120799:31120799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776284688 |
| CDS Mutation | c.4345C>T |
| AA Mutation | p.Arg1449Trp(p.R1449W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31210080:31210080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764516098 |
| CDS Mutation | c.2353G>A |
| AA Mutation | p.Asp785Asn(p.D785N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31252107:31252107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1046G>A |
| AA Mutation | p.Arg349Gln(p.R349Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31154294:31154294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747060840 |
| CDS Mutation | c.3124C>T |
| AA Mutation | p.Arg1042Cys(p.R1042C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31266034:31266034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.939A>C |
| AA Mutation | p.Gln313His(p.Q313H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31182466:31182466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2842G>T |
| AA Mutation | p.Ala948Ser(p.A948S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31266482:31266482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.491G>T |
| AA Mutation | p.Ser164Ile(p.S164I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31130242:31130242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4016C>T |
| AA Mutation | p.Ala1339Val(p.A1339V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31146917:31146917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3453A>C |
| AA Mutation | p.Lys1151Asn(p.K1151N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31251838:31251838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1315G>A |
| AA Mutation | p.Ala439Thr(p.A439T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31120505:31120505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4639G>A |
| AA Mutation | p.Ala1547Thr(p.A1547T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000286827 |
| Start | 31245631:31245631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756834470 |
| CDS Mutation | c.1441G>A |
| AA Mutation | p.Gly481Ser(p.G481S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31266865:31266865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144300474 |
| CDS Mutation | c.108G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31266640:31266640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200120014 |
| CDS Mutation | c.333C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31251839:31251839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1314C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31135973:31135973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143123730 |
| CDS Mutation | c.3843G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31124580:31124580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4248T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31130247:31130247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767412686 |
| CDS Mutation | c.4011G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31251884:31251884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1269G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31251893:31251893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1260G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31245632:31245632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745535556 |
| CDS Mutation | c.1440C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31120440:31120440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755574864 |
| CDS Mutation | c.4704C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000286827 |
| Start | 31223418:31223418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs186818915 |
| CDS Mutation | c.1983G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |