Primary Site >> Stomach Cancer
Gene >> NBAS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15474101:15474101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555950436 |
| CDS Mutation | c.1565G>A |
| AA Mutation | p.Arg522His(p.R522H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15402250:15402250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2989G>A |
| AA Mutation | p.Glu997Lys(p.E997K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15461327:15461327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2213T>C |
| AA Mutation | p.Val738Ala(p.V738A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15186817:15186817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779958737 |
| CDS Mutation | c.6636C>A |
| AA Mutation | p.Asn2212Lys(p.N2212K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15539250:15539250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.486G>A |
| AA Mutation | p.Met162Ile(p.M162I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15474294:15474294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775941838 |
| CDS Mutation | c.1372C>T |
| AA Mutation | p.Arg458Cys(p.R458C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15474102:15474102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187987936 |
| CDS Mutation | c.1564C>T |
| AA Mutation | p.Arg522Cys(p.R522C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000281513 |
| Start | 15467405:15467405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2021T>C |
| AA Mutation | p.Leu674Ser(p.L674S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15467712:15467712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1970A>T |
| AA Mutation | p.Lys657Met(p.K657M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15275521:15275521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745755293 |
| CDS Mutation | c.5687T>C |
| AA Mutation | p.Val1896Ala(p.V1896A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15417672:15417672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372807975 |
| CDS Mutation | c.2618G>A |
| AA Mutation | p.Arg873Gln(p.R873Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15539288:15539288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.448G>A |
| AA Mutation | p.Ala150Thr(p.A150T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15218894:15218894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773412024 |
| CDS Mutation | c.6311G>A |
| AA Mutation | p.Arg2104Gln(p.R2104Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15275690:15275690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5518A>G |
| AA Mutation | p.Met1840Val(p.M1840V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15461294:15461294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544578792 |
| CDS Mutation | c.2246G>A |
| AA Mutation | p.Gly749Asp(p.G749D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15167166:15167166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6998A>C |
| AA Mutation | p.His2333Pro(p.H2333P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15238664:15238664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5747A>G |
| AA Mutation | p.Glu1916Gly(p.E1916G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15218865:15218865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6340G>A |
| AA Mutation | p.Gly2114Arg(p.G2114R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000281513 |
| Start | 15556801:15556801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772268045 |
| CDS Mutation | c.191G>A |
| AA Mutation | p.Arg64His(p.R64H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000281513 |
| Start | 15277017:15277017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5223G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000281513 |
| Start | 15427728:15427728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748466608 |
| CDS Mutation | c.2406C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000281513 |
| Start | 15473300:15473300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138310172 |
| CDS Mutation | c.1647C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000281513 |
| Start | 15167243:15167243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6921C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000281513 |
| Start | 15554075:15554075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.273T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000281513 |
| Start | 15504155:15504155(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.944delG |
| AA Mutation | p.Gly315AspfsTer10(p.G315Dfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000281513 |
| Start | 15478232:15478232(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs772472509 |
| CDS Mutation | c.1141delA |
| AA Mutation | p.Ile381SerfsTer10(p.I381Sfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000281513 |
| Start | 15474300:15474300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372603397 |
| CDS Mutation | c.1366C>T |
| AA Mutation | p.Arg456Ter(p.R456*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000281513 |
| Start | 15475815:15475815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376113678 |
| CDS Mutation | c.1213C>T |
| AA Mutation | p.Arg405Ter(p.R405*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000281513 |
| Start | 15536446:15536446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.619C>T |
| AA Mutation | p.Arg207Ter(p.R207*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | stop_gained;protein_altering_variant |
| Transcription ID | ENST00000281513 |
| Start | 15402294:15402295(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2944_2945insTGTTAGAAT |
| AA Mutation | p.Gln982delinsLeuLeuGluTer(p.Q982delinsLLE*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000281513 |
| Start | 15475810:15475810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1218C>A |
| AA Mutation | p.Cys406Ter(p.C406*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000281513 |
| Start | 15474121:15474122(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1544dupA |
| AA Mutation | p.Asn515LysfsTer21(p.N515Kfs*21) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000281513 |
| Start | 15374719:15374720(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3591_3592insAATACTAGTAAAT |
| AA Mutation | p.Cys1198AsnfsTer31(p.C1198Nfs*31) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000281513 |
| Start | 15478231:15478232(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs780670508 |
| CDS Mutation | c.1141dupA |
| AA Mutation | p.Ile381AsnfsTer4(p.I381Nfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |