Primary Site >> Stomach Cancer
Gene >> UTRN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144840811:144840811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10249A>G |
| AA Mutation | p.Ser3417Gly(p.S3417G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144537645:144537645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6297G>C |
| AA Mutation | p.Trp2099Cys(p.W2099C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144447681:144447681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1802T>G |
| AA Mutation | p.Leu601Arg(p.L601R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144479926:144479926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375499592 |
| CDS Mutation | c.3451C>T |
| AA Mutation | p.Arg1151Trp(p.R1151W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144511102:144511102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4923A>C |
| AA Mutation | p.Glu1641Asp(p.E1641D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144793926:144793926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9013C>A |
| AA Mutation | p.Leu3005Ile(p.L3005I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144493451:144493451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771082025 |
| CDS Mutation | c.4588G>A |
| AA Mutation | p.Ala1530Thr(p.A1530T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144516329:144516329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5345T>A |
| AA Mutation | p.Ile1782Lys(p.I1782K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144490132:144490132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151173089 |
| CDS Mutation | c.4196G>A |
| AA Mutation | p.Arg1399His(p.R1399H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144438822:144438822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761620103 |
| CDS Mutation | c.1319G>A |
| AA Mutation | p.Arg440His(p.R440H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144835793:144835793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746232110 |
| CDS Mutation | c.9679G>A |
| AA Mutation | p.Ala3227Thr(p.A3227T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144754765:144754765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8401G>C |
| AA Mutation | p.Asp2801His(p.D2801H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144577154:144577154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749768508 |
| CDS Mutation | c.7345C>T |
| AA Mutation | p.Arg2449Cys(p.R2449C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144479929:144479929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3454G>T |
| AA Mutation | p.Asp1152Tyr(p.D1152Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144479952:144479952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3477A>C |
| AA Mutation | p.Glu1159Asp(p.E1159D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144487575:144487575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3850G>A |
| AA Mutation | p.Ala1284Thr(p.A1284T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144539400:144539400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6476A>C |
| AA Mutation | p.Lys2159Thr(p.K2159T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144548847:144548847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150069642 |
| CDS Mutation | c.6803G>A |
| AA Mutation | p.Arg2268Gln(p.R2268Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144533093:144533093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6066G>T |
| AA Mutation | p.Glu2022Asp(p.E2022D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144782052:144782052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8763G>A |
| AA Mutation | p.Met2921Ile(p.M2921I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144429677:144429677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750839546 |
| CDS Mutation | c.791G>A |
| AA Mutation | p.Arg264His(p.R264H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144514699:144514699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115466543 |
| CDS Mutation | c.5123G>A |
| AA Mutation | p.Arg1708His(p.R1708H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144803095:144803095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776348759 |
| CDS Mutation | c.9305G>A |
| AA Mutation | p.Arg3102Gln(p.R3102Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367545 |
| Start | 144793836:144793836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8923C>T |
| AA Mutation | p.Leu2975Phe(p.L2975F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144523041:144523041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5759T>G |
| AA Mutation | p.Leu1920Arg(p.L1920R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144557199:144557199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7177G>A |
| AA Mutation | p.Ala2393Thr(p.A2393T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144462739:144462739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2939C>A |
| AA Mutation | p.Pro980His(p.P980H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144797944:144797944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9199C>A |
| AA Mutation | p.Gln3067Lys(p.Q3067K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144748482:144748482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8176G>A |
| AA Mutation | p.Asp2726Asn(p.D2726N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144751911:144751911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8314C>T |
| AA Mutation | p.Arg2772Cys(p.R2772C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144491019:144491019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4354G>A |
| AA Mutation | p.Asp1452Asn(p.D1452N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144435978:144435978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.899C>T |
| AA Mutation | p.Thr300Ile(p.T300I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144479878:144479878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757958729 |
| CDS Mutation | c.3403G>A |
| AA Mutation | p.Ala1135Thr(p.A1135T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144462684:144462684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750447450 |
| CDS Mutation | c.2884C>A |
| AA Mutation | p.Pro962Thr(p.P962T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144482300:144482300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3599G>A |
| AA Mutation | p.Gly1200Asp(p.G1200D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144459285:144459285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376535714 |
| CDS Mutation | c.2638G>A |
| AA Mutation | p.Asp880Asn(p.D880N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144827368:144827368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9515T>A |
| AA Mutation | p.Met3172Lys(p.M3172K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144836411:144836411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9935C>T |
| AA Mutation | p.Ser3312Leu(p.S3312L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144554876:144554876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7117C>A |
| AA Mutation | p.Gln2373Lys(p.Q2373K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144458927:144458927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2442C>G |
| AA Mutation | p.Ile814Met(p.I814M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367545 |
| Start | 144459334:144459334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115273171 |
| CDS Mutation | c.2687G>A |
| AA Mutation | p.Arg896His(p.R896H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144577141:144577141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754442261 |
| CDS Mutation | c.7332G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144793841:144793841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8928T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144403136:144403136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754635241 |
| CDS Mutation | c.93C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144678456:144678456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150099766 |
| CDS Mutation | c.7530C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144426337:144426337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.456T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144835789:144835789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9675G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144789236:144789236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8877A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144437609:144437609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1104C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144448605:144448605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1908T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144482259:144482259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3558G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144479859:144479859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112708396 |
| CDS Mutation | c.3384G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367545 |
| Start | 144291864:144291864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181012386 |
| CDS Mutation | c.36C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367545 |
| Start | 144461335:144461335(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2852delA |
| AA Mutation | p.Lys951ArgfsTer32(p.K951Rfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367545 |
| Start | 144438844:144438844(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1345delC |
| AA Mutation | p.Leu449TrpfsTer5(p.L449Wfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000367545 |
| Start | 144840833:144840833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141700678 |
| CDS Mutation | c.10270+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | splice_acceptor_variant;intron_variant |
| Transcription ID | ENST00000367545 |
| Start | 144771892:144771905(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.8496-15_8496-2delACCTTTTTTTTCCA |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |