Primary Site >> Stomach Cancer
Gene >> HOOK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397668 |
| Start | 12773028:12773028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371935053 |
| CDS Mutation | c.221T>C |
| AA Mutation | p.Met74Thr(p.M74T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397668 |
| Start | 12763289:12763289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2153A>C |
| AA Mutation | p.Lys718Thr(p.K718T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397668 |
| Start | 12771285:12771285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202071884 |
| CDS Mutation | c.635C>T |
| AA Mutation | p.Ala212Val(p.A212V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397668 |
| Start | 12764837:12764837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754972063 |
| CDS Mutation | c.1804C>T |
| AA Mutation | p.Arg602Cys(p.R602C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397668 |
| Start | 12767420:12767420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1348G>A |
| AA Mutation | p.Ala450Thr(p.A450T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397668 |
| Start | 12766155:12766155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1459C>T |
| AA Mutation | p.Arg487Cys(p.R487C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397668 |
| Start | 12772659:12772659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112046714 |
| CDS Mutation | c.410C>T |
| AA Mutation | p.Thr137Met(p.T137M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397668 |
| Start | 12771468:12771468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.529T>C |
| AA Mutation | p.Tyr177His(p.Y177H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397668 |
| Start | 12765047:12765047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1675A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397668 |
| Start | 12772904:12772904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767313667 |
| CDS Mutation | c.264G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397668 |
| Start | 12765954:12765954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1572G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397668 |
| Start | 12771206:12771206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.714G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397668 |
| Start | 12765940:12765940(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs768806444 |
| CDS Mutation | c.1586delG |
| AA Mutation | p.Gly529AlafsTer11(p.G529Afs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000397668 |
| Start | 12766001:12766001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1525C>T |
| AA Mutation | p.Gln509Ter(p.Q509*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |