Primary Site >> Stomach Cancer
Gene >> SLIT2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20528997:20528997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1511T>A |
| AA Mutation | p.Leu504Gln(p.L504Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20511071:20511071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.992T>C |
| AA Mutation | p.Leu331Pro(p.L331P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20524055:20524055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1316A>G |
| AA Mutation | p.Lys439Arg(p.K439R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20596651:20596651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3557T>G |
| AA Mutation | p.Leu1186Arg(p.L1186R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20524028:20524028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1289A>C |
| AA Mutation | p.Asn430Thr(p.N430T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20567354:20567354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2818T>G |
| AA Mutation | p.Phe940Val(p.F940V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20480726:20480726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.478T>C |
| AA Mutation | p.Tyr160His(p.Y160H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20519438:20519438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1115T>C |
| AA Mutation | p.Phe372Ser(p.F372S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20595744:20595744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3230T>G |
| AA Mutation | p.Phe1077Cys(p.F1077C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20618837:20618837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4418C>G |
| AA Mutation | p.Thr1473Arg(p.T1473R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20488851:20488851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.644G>A |
| AA Mutation | p.Cys215Tyr(p.C215Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20529069:20529069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1583C>T |
| AA Mutation | p.Pro528Leu(p.P528L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20596554:20596554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3460G>A |
| AA Mutation | p.Glu1154Lys(p.E1154K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20617050:20617050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3988T>G |
| AA Mutation | p.Leu1330Val(p.L1330V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000504154 |
| Start | 20531986:20531986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1616G>A |
| AA Mutation | p.Arg539His(p.R539H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20617475:20617475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4173C>A |
| AA Mutation | p.Phe1391Leu(p.F1391L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20618857:20618857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4438T>A |
| AA Mutation | p.Leu1480Ile(p.L1480I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20524169:20524169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192894188 |
| CDS Mutation | c.1430G>A |
| AA Mutation | p.Arg477His(p.R477H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20253883:20253883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.68T>A |
| AA Mutation | p.Val23Glu(p.V23E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20533604:20533604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1721A>G |
| AA Mutation | p.Glu574Gly(p.E574G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20589727:20589727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3172A>G |
| AA Mutation | p.Lys1058Glu(p.K1058E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20519419:20519419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1096A>G |
| AA Mutation | p.Ser366Gly(p.S366G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20598349:20598349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747000768 |
| CDS Mutation | c.3646C>T |
| AA Mutation | p.Arg1216Cys(p.R1216C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20553813:20553813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2570G>A |
| AA Mutation | p.Gly857Glu(p.G857E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20595810:20595810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757036981 |
| CDS Mutation | c.3296C>T |
| AA Mutation | p.Thr1099Met(p.T1099M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20486262:20486262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.602T>G |
| AA Mutation | p.Leu201Arg(p.L201R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20610121:20610121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3801G>C |
| AA Mutation | p.Leu1267Phe(p.L1267F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20617165:20617165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4103A>T |
| AA Mutation | p.Asp1368Val(p.D1368V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20491784:20491784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.799T>G |
| AA Mutation | p.Ser267Ala(p.S267A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20253946:20253946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.131T>G |
| AA Mutation | p.Leu44Arg(p.L44R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20567303:20567303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2767C>A |
| AA Mutation | p.Leu923Ile(p.L923I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20618809:20618809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4390A>C |
| AA Mutation | p.Lys1464Gln(p.K1464Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20256683:20256683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772070012 |
| CDS Mutation | c.191G>A |
| AA Mutation | p.Gly64Glu(p.G64E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20523878:20523878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1249T>G |
| AA Mutation | p.Ser417Ala(p.S417A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000504154 |
| Start | 20524105:20524105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1366C>T |
| AA Mutation | p.Arg456Cys(p.R456C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20491888:20491888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.903C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20533653:20533653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373575007 |
| CDS Mutation | c.1770G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20618961:20618961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746191825 |
| CDS Mutation | c.4542C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20519385:20519385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1062C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20595811:20595811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750603170 |
| CDS Mutation | c.3297G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20486203:20486203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.543T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20486236:20486236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.576G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20595748:20595748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573018203 |
| CDS Mutation | c.3234C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20532044:20532044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1674T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20568979:20568979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3063A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000504154 |
| Start | 20595733:20595733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372434910 |
| CDS Mutation | c.3219C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000504154 |
| Start | 20553950:20553950(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2712delA |
| AA Mutation | p.Lys904AsnfsTer13(p.K904Nfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000504154 |
| Start | 20510517:20510518(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.938_939delAA |
| AA Mutation | p.Lys313SerfsTer11(p.K313Sfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000504154 |
| Start | 20467815:20467815(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.464delA |
| AA Mutation | p.Asn155IlefsTer88(p.N155Ifs*88) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |