Primary Site >> Stomach Cancer
Gene >> IQGAP3
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000361170 |
| Start | 156550263:156550263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1823G>T |
| AA Mutation | p.Arg608Ile(p.R608I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156563640:156563640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200764066 |
| CDS Mutation | c.532G>A |
| AA Mutation | p.Glu178Lys(p.E178K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156566397:156566397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs191829043 |
| CDS Mutation | c.275G>A |
| AA Mutation | p.Arg92Gln(p.R92Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156563154:156563154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190122865 |
| CDS Mutation | c.778G>A |
| AA Mutation | p.Ala260Thr(p.A260T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156554368:156554368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748702160 |
| CDS Mutation | c.1315G>A |
| AA Mutation | p.Val439Met(p.V439M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156540722:156540722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368663938 |
| CDS Mutation | c.2725C>T |
| AA Mutation | p.Arg909Trp(p.R909W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156526590:156526590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4792C>A |
| AA Mutation | p.Gln1598Lys(p.Q1598K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156526493:156526493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140982853 |
| CDS Mutation | c.4889G>A |
| AA Mutation | p.Arg1630Gln(p.R1630Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156548668:156548668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771267264 |
| CDS Mutation | c.1906G>A |
| AA Mutation | p.Ala636Thr(p.A636T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156537245:156537245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374568868 |
| CDS Mutation | c.3358C>T |
| AA Mutation | p.Arg1120Cys(p.R1120C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000361170 |
| Start | 156562587:156562587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751509407 |
| CDS Mutation | c.877G>A |
| AA Mutation | p.Val293Ile(p.V293I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361170 |
| Start | 156528950:156528950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772944929 |
| CDS Mutation | c.4537C>T |
| AA Mutation | p.Arg1513Trp(p.R1513W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361170 |
| Start | 156566045:156566045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.342C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361170 |
| Start | 156529008:156529008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4479C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361170 |
| Start | 156548741:156548741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1833T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361170 |
| Start | 156538832:156538832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3258T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361170 |
| Start | 156534120:156534120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3762C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361170 |
| Start | 156551744:156551744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1695C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361170 |
| Start | 156554300:156554300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1383C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361170 |
| Start | 156548136:156548136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2241G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361170 |
| Start | 156564654:156564654(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.398delA |
| AA Mutation | p.Lys133ArgfsTer6(p.K133Rfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000361170 |
| Start | 156563211:156563211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755115439 |
| CDS Mutation | c.721C>T |
| AA Mutation | p.Arg241Ter(p.R241*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |