Primary Site >> Stomach Cancer
Gene >> TENM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124420529:124420529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4743C>A |
| AA Mutation | p.Ser1581Arg(p.S1581R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124503634:124503634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3371A>C |
| AA Mutation | p.Gln1124Pro(p.Q1124P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124420585:124420585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4687G>A |
| AA Mutation | p.Asp1563Asn(p.D1563N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124422279:124422279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4443T>G |
| AA Mutation | p.Cys1481Trp(p.C1481W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124405222:124405222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745904541 |
| CDS Mutation | c.5179C>T |
| AA Mutation | p.Arg1727Cys(p.R1727C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124651945:124651945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1548G>A |
| AA Mutation | p.Met516Ile(p.M516I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124652091:124652091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1402C>A |
| AA Mutation | p.Leu468Met(p.L468M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124653633:124653633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1319C>A |
| AA Mutation | p.Ser440Tyr(p.S440Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124385902:124385902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5830A>G |
| AA Mutation | p.Thr1944Ala(p.T1944A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124384398:124384398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762426434 |
| CDS Mutation | c.6512G>A |
| AA Mutation | p.Arg2171His(p.R2171H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124422371:124422371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746639113 |
| CDS Mutation | c.4351C>T |
| AA Mutation | p.Arg1451Cys(p.R1451C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124547040:124547040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2485T>A |
| AA Mutation | p.Tyr829Asn(p.Y829N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124384063:124384063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6847T>G |
| AA Mutation | p.Leu2283Val(p.L2283V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124523396:124523396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3001C>T |
| AA Mutation | p.Pro1001Ser(p.P1001S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124737111:124737111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.622A>C |
| AA Mutation | p.Lys208Gln(p.K208Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124385988:124385988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5744C>T |
| AA Mutation | p.Thr1915Ile(p.T1915I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124422524:124422524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4198G>A |
| AA Mutation | p.Ala1400Thr(p.A1400T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124497258:124497258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3453A>G |
| AA Mutation | p.Ile1151Met(p.I1151M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124894325:124894325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.506A>C |
| AA Mutation | p.Asp169Ala(p.D169A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124380982:124380982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7732C>A |
| AA Mutation | p.Leu2578Ile(p.L2578I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124392164:124392164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5555C>T |
| AA Mutation | p.Thr1852Met(p.T1852M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124523506:124523506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2891T>G |
| AA Mutation | p.Val964Gly(p.V964G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124645225:124645225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1794T>A |
| AA Mutation | p.Asp598Glu(p.D598E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124406479:124406479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377378434 |
| CDS Mutation | c.4972G>A |
| AA Mutation | p.Glu1658Lys(p.E1658K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124547025:124547025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2500T>C |
| AA Mutation | p.Cys834Arg(p.C834R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124520564:124520564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3254A>C |
| AA Mutation | p.Lys1085Thr(p.K1085T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124406349:124406349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377115628 |
| CDS Mutation | c.5102C>T |
| AA Mutation | p.Thr1701Met(p.T1701M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124481839:124481839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3821A>T |
| AA Mutation | p.Lys1274Met(p.K1274M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124392147:124392147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5572A>G |
| AA Mutation | p.Thr1858Ala(p.T1858A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124645245:124645245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1774C>A |
| AA Mutation | p.Pro592Thr(p.P592T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124384630:124384630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6280A>G |
| AA Mutation | p.Thr2094Ala(p.T2094A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124895985:124895985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.474A>C |
| AA Mutation | p.Glu158Asp(p.E158D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124705189:124705189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.839A>G |
| AA Mutation | p.Tyr280Cys(p.Y280C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124481960:124481960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3700A>C |
| AA Mutation | p.Ser1234Arg(p.S1234R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124896185:124896185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274C>A |
| AA Mutation | p.His92Asn(p.H92N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124383795:124383795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7115A>G |
| AA Mutation | p.His2372Arg(p.H2372R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124392224:124392224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5495G>T |
| AA Mutation | p.Trp1832Leu(p.W1832L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124384083:124384083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6827A>G |
| AA Mutation | p.Asn2276Ser(p.N2276S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124422338:124422338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4384T>C |
| AA Mutation | p.Tyr1462His(p.Y1462H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124381044:124381044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7670C>T |
| AA Mutation | p.Ala2557Val(p.A2557V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124384138:124384138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377058853 |
| CDS Mutation | c.6772G>A |
| AA Mutation | p.Ala2258Thr(p.A2258T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371130 |
| Start | 124405234:124405234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5167G>A |
| AA Mutation | p.Asp1723Asn(p.D1723N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124384118:124384118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6792G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124561783:124561783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776544734 |
| CDS Mutation | c.2322A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124894345:124894345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.486A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124705023:124705023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1005C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124529869:124529869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2766T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124520560:124520560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771756486 |
| CDS Mutation | c.3258C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124420634:124420634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4638G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124420538:124420538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748565386 |
| CDS Mutation | c.4734G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124406369:124406369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5082C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124641855:124641855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749364562 |
| CDS Mutation | c.2013T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124523445:124523445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2952A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371130 |
| Start | 124422516:124422516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4206C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371130 |
| Start | 124963718:124963718(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.36delA |
| AA Mutation | p.Pro13GlnfsTer9(p.P13Qfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000371130 |
| Start | 124671684:124671684(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1167delA |
| AA Mutation | p.Val390CysfsTer8(p.V390Cfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000371130 |
| Start | 124523576:124523576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780679877 |
| CDS Mutation | c.2821C>T |
| AA Mutation | p.Arg941Ter(p.R941*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |