Primary Site >> Stomach Cancer
Gene >> INCENP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394818 |
| Start | 62130553:62130553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1026G>C |
| AA Mutation | p.Lys342Asn(p.K342N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394818 |
| Start | 62148540:62148540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2269G>A |
| AA Mutation | p.Glu757Lys(p.E757K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394818 |
| Start | 62130290:62130290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.763T>C |
| AA Mutation | p.Ser255Pro(p.S255P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394818 |
| Start | 62130360:62130360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs77555538 |
| CDS Mutation | c.833G>A |
| AA Mutation | p.Arg278Gln(p.R278Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394818 |
| Start | 62130090:62130090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.563C>A |
| AA Mutation | p.Ser188Tyr(p.S188Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394818 |
| Start | 62129934:62129934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.407T>C |
| AA Mutation | p.Met136Thr(p.M136T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394818 |
| Start | 62130402:62130402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751814772 |
| CDS Mutation | c.875C>T |
| AA Mutation | p.Thr292Met(p.T292M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394818 |
| Start | 62145039:62145039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200313762 |
| CDS Mutation | c.1663C>T |
| AA Mutation | p.Arg555Cys(p.R555C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000394818 |
| Start | 62141509:62141509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762472113 |
| CDS Mutation | c.1603G>A |
| AA Mutation | p.Val535Ile(p.V535I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000394818 |
| Start | 62130336:62130336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.809C>A |
| AA Mutation | p.Pro270Gln(p.P270Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394818 |
| Start | 62150089:62150089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2424G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394818 |
| Start | 62140743:62140743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746596653 |
| CDS Mutation | c.1383C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000394818 |
| Start | 62151808:62151808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771720381 |
| CDS Mutation | c.2589G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |