Primary Site >> Stomach Cancer
Gene >> IPO13
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372343 |
| Start | 43964275:43964275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2351G>A |
| AA Mutation | p.Arg784Lys(p.R784K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372343 |
| Start | 43949714:43949714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.382G>A |
| AA Mutation | p.Ala128Thr(p.A128T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372343 |
| Start | 43956397:43956397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.899G>T |
| AA Mutation | p.Gly300Val(p.G300V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372343 |
| Start | 43949537:43949537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775594295 |
| CDS Mutation | c.205G>A |
| AA Mutation | p.Asp69Asn(p.D69N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372343 |
| Start | 43961220:43961220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2302T>A |
| AA Mutation | p.Phe768Ile(p.F768I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372343 |
| Start | 43967450:43967450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183495352 |
| CDS Mutation | c.2749C>T |
| AA Mutation | p.Arg917Cys(p.R917C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372343 |
| Start | 43949849:43949849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.517C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372343 |
| Start | 43958812:43958812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1951C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372343 |
| Start | 43956683:43956683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1086C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372343 |
| Start | 43967371:43967371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563338901 |
| CDS Mutation | c.2670C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372343 |
| Start | 43958565:43958565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1854C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372343 |
| Start | 43966992:43966992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2586T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000372343 |
| Start | 43966611:43966611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751137210 |
| CDS Mutation | c.2434C>T |
| AA Mutation | p.Arg812Ter(p.R812*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |