Primary Site >> Stomach Cancer
Gene >> ATG9B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000469530 |
| Start | 151023490:151023490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.614G>A |
| AA Mutation | p.Arg205Gln(p.R205Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000469530 |
| Start | 151017197:151017197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570781096 |
| CDS Mutation | c.2128C>T |
| AA Mutation | p.Arg710Trp(p.R710W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000469530 |
| Start | 151017161:151017161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2164G>T |
| AA Mutation | p.Gly722Trp(p.G722W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000469530 |
| Start | 151018702:151018702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1636A>G |
| AA Mutation | p.Thr546Ala(p.T546A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000469530 |
| Start | 151023111:151023111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.755C>A |
| AA Mutation | p.Pro252His(p.P252H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000469530 |
| Start | 151024176:151024176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.248C>T |
| AA Mutation | p.Ala83Val(p.A83V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000469530 |
| Start | 151017229:151017229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374927452 |
| CDS Mutation | c.2096C>T |
| AA Mutation | p.Ala699Val(p.A699V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000469530 |
| Start | 151018645:151018645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1693C>T |
| AA Mutation | p.Leu565Phe(p.L565F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000469530 |
| Start | 151016738:151016738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367683605 |
| CDS Mutation | c.2373G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000469530 |
| Start | 151017252:151017252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2073T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000469530 |
| Start | 151024235:151024235(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.189delC |
| AA Mutation | p.Ser64ProfsTer42(p.S64Pfs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000469530 |
| Start | 151017163:151017163(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2162delC |
| AA Mutation | p.Pro721GlnfsTer62(p.P721Qfs*62) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |