Primary Site >> Stomach Cancer
Gene >> CIC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42292998:42292998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3512G>A |
| AA Mutation | p.Arg1171Gln(p.R1171Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42292673:42292673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3283T>G |
| AA Mutation | p.Phe1095Val(p.F1095V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42289334:42289334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1288G>A |
| AA Mutation | p.Ala430Thr(p.A430T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42287624:42287624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.662G>A |
| AA Mutation | p.Arg221His(p.R221H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42286810:42286810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.107C>T |
| AA Mutation | p.Pro36Leu(p.P36L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42289197:42289197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1151C>T |
| AA Mutation | p.Ala384Val(p.A384V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42290977:42290977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2209G>A |
| AA Mutation | p.Ala737Thr(p.A737T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42291070:42291070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2302C>A |
| AA Mutation | p.Pro768Thr(p.P768T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42289910:42289910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1423G>A |
| AA Mutation | p.Glu475Lys(p.E475K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42289851:42289851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1364A>G |
| AA Mutation | p.Asp455Gly(p.D455G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42287134:42287134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.346G>A |
| AA Mutation | p.Val116Met(p.V116M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42287203:42287203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.415C>T |
| AA Mutation | p.Arg139Trp(p.R139W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42294989:42294989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4625G>T |
| AA Mutation | p.Gly1542Val(p.G1542V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000575354 |
| Start | 42291005:42291005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2237C>T |
| AA Mutation | p.Ala746Val(p.A746V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000575354 |
| Start | 42287565:42287565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.603G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000575354 |
| Start | 42295002:42295002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4638C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000575354 |
| Start | 42287169:42287169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370589441 |
| CDS Mutation | c.381G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000575354 |
| Start | 42291009:42291009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2241A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000575354 |
| Start | 42292136:42292136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748512902 |
| CDS Mutation | c.2937G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42293224:42293224(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3743delC |
| AA Mutation | p.Pro1248HisfsTer54(p.P1248Hfs*54) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42290289:42290289(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1526delC |
| AA Mutation | p.Pro509HisfsTer14(p.P509Hfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42291457:42291457(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2694delC |
| AA Mutation | p.Ala900ProfsTer24(p.A900Pfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42292731:42292731(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3347delC |
| AA Mutation | p.Pro1116GlnfsTer45(p.P1116Qfs*45) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42287116:42287116(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.332delC |
| AA Mutation | p.Pro111HisfsTer94(p.P111Hfs*94) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42294946:42294946(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.4586delC |
| AA Mutation | p.Pro1529LeufsTer91(p.P1529Lfs*91) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42287130:42287130(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.346delG |
| AA Mutation | p.Val116TrpfsTer89(p.V116Wfs*89) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42287190:42287194(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.402_406delCCCAG |
| AA Mutation | p.Pro135ArgfsTer7(p.P135Rfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42287187:42287187(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.404delC |
| AA Mutation | p.Pro135GlnfsTer70(p.P135Qfs*70) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42290475:42290475(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1711delC |
| AA Mutation | p.Leu571TyrfsTer157(p.L571Yfs*157) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000575354 |
| Start | 42291719:42291719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2860C>T |
| AA Mutation | p.Gln954Ter(p.Q954*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000575354 |
| Start | 42290698:42290698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1930G>T |
| AA Mutation | p.Gly644Ter(p.G644*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42289009:42289010(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1057dupC |
| AA Mutation | p.Arg353ProfsTer54(p.R353Pfs*54) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42292730:42292731(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs761345552 |
| CDS Mutation | c.3347dupC |
| AA Mutation | p.Ser1117LysfsTer34(p.S1117Kfs*34) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000575354 |
| Start | 42287186:42287187(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.404dupC |
| AA Mutation | p.Gly136ArgfsTer8(p.G136Rfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |