Primary Site >> Stomach Cancer
Gene >> IRS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375856 |
| Start | 109782159:109782159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3895G>A |
| AA Mutation | p.Val1299Ile(p.V1299I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375856 |
| Start | 109782378:109782378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369041453 |
| CDS Mutation | c.3676G>A |
| AA Mutation | p.Gly1226Arg(p.G1226R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375856 |
| Start | 109784333:109784333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1721G>A |
| AA Mutation | p.Arg574Lys(p.R574K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375856 |
| Start | 109782056:109782056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3998C>T |
| AA Mutation | p.Ala1333Val(p.A1333V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375856 |
| Start | 109782168:109782168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3886G>A |
| AA Mutation | p.Ala1296Thr(p.A1296T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375856 |
| Start | 109784393:109784393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779681200 |
| CDS Mutation | c.1661G>A |
| AA Mutation | p.Arg554His(p.R554H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375856 |
| Start | 109782425:109782425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3629C>T |
| AA Mutation | p.Ala1210Val(p.A1210V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375856 |
| Start | 109784339:109784339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1715G>A |
| AA Mutation | p.Arg572His(p.R572H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375856 |
| Start | 109785754:109785754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.300C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375856 |
| Start | 109782070:109782070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775970415 |
| CDS Mutation | c.3984C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375856 |
| Start | 109784365:109784365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1689G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375856 |
| Start | 109784449:109784449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1605C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375856 |
| Start | 109782264:109782264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780308804 |
| CDS Mutation | c.3790C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000375856 |
| Start | 109782043:109782043(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4011delA |
| AA Mutation | p.Glu1338SerfsTer19(p.E1338Sfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant |
| Transcription ID | ENST00000375856 |
| Start | 109782041:109782059(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3995_4012+1delAGGCCACCATCGTGAAAGG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |