Primary Site >> Stomach Cancer
Gene >> F8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154929744:154929744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4046G>A |
| AA Mutation | p.Arg1349Lys(p.R1349K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154930006:154930006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3784G>A |
| AA Mutation | p.Ala1262Thr(p.A1262T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154899936:154899936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6203A>G |
| AA Mutation | p.Lys2068Arg(p.K2068R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154966091:154966091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1322A>T |
| AA Mutation | p.Lys441Met(p.K441M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154931023:154931023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2767T>G |
| AA Mutation | p.Leu923Val(p.L923V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154966669:154966669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1028T>C |
| AA Mutation | p.Val343Ala(p.V343A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154928742:154928742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5048A>T |
| AA Mutation | p.Tyr1683Phe(p.Y1683F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154930461:154930461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3329A>C |
| AA Mutation | p.Asn1110Thr(p.N1110T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154931224:154931224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2566T>G |
| AA Mutation | p.Phe856Val(p.F856V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154929536:154929536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4254T>G |
| AA Mutation | p.Ile1418Met(p.I1418M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154929805:154929805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781927234 |
| CDS Mutation | c.3985C>T |
| AA Mutation | p.Arg1329Cys(p.R1329C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154969417:154969417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137852404 |
| CDS Mutation | c.923C>T |
| AA Mutation | p.Ser308Leu(p.S308L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154997038:154997038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137852384 |
| CDS Mutation | c.323A>C |
| AA Mutation | p.Lys108Thr(p.K108T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154931349:154931349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782158350 |
| CDS Mutation | c.2441G>A |
| AA Mutation | p.Arg814Gln(p.R814Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154997041:154997041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.320T>G |
| AA Mutation | p.Leu107Arg(p.L107R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154902119:154902119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6047G>A |
| AA Mutation | p.Arg2016Gln(p.R2016Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154929630:154929630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4160C>T |
| AA Mutation | p.Ser1387Phe(p.S1387F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154863136:154863136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6521A>G |
| AA Mutation | p.His2174Arg(p.H2174R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360256 |
| Start | 154957034:154957034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1675G>A |
| AA Mutation | p.Glu559Lys(p.E559K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360256 |
| Start | 154928813:154928813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4977A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360256 |
| Start | 154931621:154931621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2169C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360256 |
| Start | 154931198:154931198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2592G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360256 |
| Start | 154902142:154902142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6024A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360256 |
| Start | 154929293:154929293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4497C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360256 |
| Start | 154966081:154966081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1332A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360256 |
| Start | 154929920:154929920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782292361 |
| CDS Mutation | c.3870A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360256 |
| Start | 154860450:154860450(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6882delT |
| AA Mutation | p.Gln2295ArgfsTer5(p.Q2295Rfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360256 |
| Start | 154863192:154863192(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6465delA |
| AA Mutation | p.Lys2155AsnfsTer31(p.K2155Nfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360256 |
| Start | 154929920:154929920(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3870delA |
| AA Mutation | p.Glu1292ArgfsTer16(p.E1292Rfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360256 |
| Start | 154930153:154930153(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs387906450 |
| CDS Mutation | c.3637delA |
| AA Mutation | p.Ile1213PhefsTer5(p.I1213Ffs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360256 |
| Start | 154929411:154929411(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs387906455 |
| CDS Mutation | c.4379delA |
| AA Mutation | p.Asn1460IlefsTer5(p.N1460Ifs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000360256 |
| Start | 154957133:154957133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1576G>T |
| AA Mutation | p.Glu526Ter(p.E526*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360256 |
| Start | 154928964:154928965(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs397514036 |
| CDS Mutation | c.4825dupA |
| AA Mutation | p.Thr1609AsnfsTer4(p.T1609Nfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |