Primary Site >> Stomach Cancer
Gene >> SIGLEC12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291707 |
| Start | 51500267:51500267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.461A>C |
| AA Mutation | p.Glu154Ala(p.E154A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291707 |
| Start | 51496953:51496953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374018929 |
| CDS Mutation | c.1526C>T |
| AA Mutation | p.Ser509Leu(p.S509L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291707 |
| Start | 51497391:51497391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1460C>T |
| AA Mutation | p.Ala487Val(p.A487V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291707 |
| Start | 51499980:51499980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.748G>A |
| AA Mutation | p.Val250Met(p.V250M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291707 |
| Start | 51499183:51499183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1122A>T |
| AA Mutation | p.Gln374His(p.Q374H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291707 |
| Start | 51498229:51498229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1194C>A |
| AA Mutation | p.His398Gln(p.H398Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291707 |
| Start | 51499191:51499191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1114G>T |
| AA Mutation | p.Val372Phe(p.V372F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000291707 |
| Start | 51499585:51499585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201888334 |
| CDS Mutation | c.940G>A |
| AA Mutation | p.Val314Met(p.V314M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291707 |
| Start | 51499616:51499616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148225737 |
| CDS Mutation | c.909G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291707 |
| Start | 51496910:51496910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145034575 |
| CDS Mutation | c.1569C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291707 |
| Start | 51499559:51499559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.966T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000291707 |
| Start | 51491677:51491677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532504299 |
| CDS Mutation | c.1752C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000291707 |
| Start | 51501582:51501582(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.152delA |
| AA Mutation | p.Asn51MetfsTer20(p.N51Mfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000291707 |
| Start | 51499453:51499453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755724495 |
| CDS Mutation | c.1072C>T |
| AA Mutation | p.Arg358Ter(p.R358*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |