Primary Site >> Pancreatic Cancer
Gene >> MUC16
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8959656:8959656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200898366 |
| CDS Mutation | c.17114C>T |
| AA Mutation | p.Ala5705Val(p.A5705V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8946464:8946464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.30306G>T |
| AA Mutation | p.Met10102Ile(p.M10102I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8979271:8979271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs576260781 |
| CDS Mutation | c.1868C>A |
| AA Mutation | p.Thr623Lys(p.T623K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8974766:8974766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6373G>T |
| AA Mutation | p.Ala2125Ser(p.A2125S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8948182:8948182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.28588G>C |
| AA Mutation | p.Glu9530Gln(p.E9530Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8915565:8915565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760969863 |
| CDS Mutation | c.36745C>T |
| AA Mutation | p.Arg12249Cys(p.R12249C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8937291:8937291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.33664T>C |
| AA Mutation | p.Phe11222Leu(p.F11222L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8863316:8863316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.42679C>A |
| AA Mutation | p.Leu14227Met(p.L14227M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8863400:8863400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750000661 |
| CDS Mutation | c.42595C>T |
| AA Mutation | p.Arg14199Trp(p.R14199W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8871545:8871545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.42054G>T |
| AA Mutation | p.Gln14018His(p.Q14018H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000397910 |
| Start | 8884959:8884959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.41353G>A |
| AA Mutation | p.Ala13785Thr(p.A13785T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8886478:8886478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.41042G>A |
| AA Mutation | p.Gly13681Asp(p.G13681D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8888871:8888871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.40628C>T |
| AA Mutation | p.Ala13543Val(p.A13543V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000397910 |
| Start | 8889890:8889890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.40418C>T |
| AA Mutation | p.Thr13473Ile(p.T13473I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8891485:8891485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.40343C>T |
| AA Mutation | p.Thr13448Ile(p.T13448I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8904988:8904988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.38159G>A |
| AA Mutation | p.Gly12720Asp(p.G12720D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8935479:8935479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.35476C>A |
| AA Mutation | p.Leu11826Ile(p.L11826I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8935647:8935647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.35308A>G |
| AA Mutation | p.Thr11770Ala(p.T11770A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8936429:8936429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.34526T>G |
| AA Mutation | p.Phe11509Cys(p.F11509C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8937117:8937117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.33838A>G |
| AA Mutation | p.Thr11280Ala(p.T11280A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8937603:8937603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.33352C>A |
| AA Mutation | p.Leu11118Ile(p.L11118I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8946838:8946838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751183092 |
| CDS Mutation | c.29932G>T |
| AA Mutation | p.Ala9978Ser(p.A9978S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8947807:8947807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182912100 |
| CDS Mutation | c.28963A>G |
| AA Mutation | p.Thr9655Ala(p.T9655A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8949445:8949445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.27325A>T |
| AA Mutation | p.Thr9109Ser(p.T9109S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8950453:8950453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.26317A>G |
| AA Mutation | p.Ile8773Val(p.I8773V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8951841:8951841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.24929G>T |
| AA Mutation | p.Arg8310Met(p.R8310M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8960058:8960058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16712C>T |
| AA Mutation | p.Thr5571Ile(p.T5571I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8980023:8980023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1116G>T |
| AA Mutation | p.Glu372Asp(p.E372D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8952393:8952393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.24377C>T |
| AA Mutation | p.Thr8126Ile(p.T8126I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8895042:8895042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746951194 |
| CDS Mutation | c.39688G>A |
| AA Mutation | p.Gly13230Arg(p.G13230R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8963325:8963325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377647571 |
| CDS Mutation | c.13445C>T |
| AA Mutation | p.Ala4482Val(p.A4482V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8953630:8953630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.23140C>T |
| AA Mutation | p.Pro7714Ser(p.P7714S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397910 |
| Start | 8954250:8954250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.22520C>T |
| AA Mutation | p.Ala7507Val(p.A7507V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397910 |
| Start | 8960561:8960561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373387179 |
| CDS Mutation | c.16209G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397910 |
| Start | 8937175:8937175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149660691 |
| CDS Mutation | c.33780G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397910 |
| Start | 8945600:8945600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.31170G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397910 |
| Start | 8956106:8956106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547807971 |
| CDS Mutation | c.20664G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397910 |
| Start | 8962310:8962310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14460T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397910 |
| Start | 8964359:8964359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12411C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397910 |
| Start | 8974179:8974179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6960C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397910 |
| Start | 8978847:8978847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2292G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397910 |
| Start | 8979495:8979495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1644C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397910 |
| Start | 8948705:8948705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.28065C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397910 |
| Start | 8975766:8975781(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5358_5373delAAGGACAGAGTCCAGC |
| AA Mutation | p.Arg1787GlnfsTer36(p.R1787Qfs*36) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000397910 |
| Start | 8938161:8938161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.32794G>T |
| AA Mutation | p.Gly10932Ter(p.G10932*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000397910 |
| Start | 8943655:8943655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.31291G>T |
| AA Mutation | p.Glu10431Ter(p.E10431*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397910 |
| Start | 8952451:8952452(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.24318dupT |
| AA Mutation | p.Glu8107Ter(p.E8107*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |