Primary Site >> Stomach Cancer
Gene >> IQGAP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76693435:76693435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148122303 |
| CDS Mutation | c.3986C>T |
| AA Mutation | p.Ala1329Val(p.A1329V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76611072:76611072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1410G>C |
| AA Mutation | p.Leu470Phe(p.L470F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76631955:76631955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1709A>G |
| AA Mutation | p.Asp570Gly(p.D570G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76695604:76695604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4144G>A |
| AA Mutation | p.Glu1382Lys(p.E1382K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76698041:76698041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4261C>T |
| AA Mutation | p.Leu1421Phe(p.L1421F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76674010:76674010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760813383 |
| CDS Mutation | c.3268G>A |
| AA Mutation | p.Asp1090Asn(p.D1090N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76695596:76695596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767513992 |
| CDS Mutation | c.4136G>A |
| AA Mutation | p.Arg1379Gln(p.R1379Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76701126:76701126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745748799 |
| CDS Mutation | c.4418C>T |
| AA Mutation | p.Ala1473Val(p.A1473V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76461666:76461666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.143A>G |
| AA Mutation | p.Lys48Arg(p.K48R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76637046:76637046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1793G>C |
| AA Mutation | p.Gly598Ala(p.G598A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76590419:76590419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.652G>T |
| AA Mutation | p.Val218Phe(p.V218F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000274364 |
| Start | 76597466:76597466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.935C>T |
| AA Mutation | p.Ala312Val(p.A312V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274364 |
| Start | 76575761:76575761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780934953 |
| CDS Mutation | c.450C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274364 |
| Start | 76658571:76658571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2433A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274364 |
| Start | 76606188:76606188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1242C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274364 |
| Start | 76693436:76693436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774651588 |
| CDS Mutation | c.3987G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000274364 |
| Start | 76695600:76695600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142258030 |
| CDS Mutation | c.4140G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000274364 |
| Start | 76631899:76631899(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1659delA |
| AA Mutation | p.Lys553AsnfsTer9(p.K553Nfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |