Primary Site >> Stomach Cancer
Gene >> TERT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310581 |
| Start | 1264558:1264558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559028617 |
| CDS Mutation | c.2689G>A |
| AA Mutation | p.Val897Met(p.V897M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310581 |
| Start | 1255294:1255294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3150G>T |
| AA Mutation | p.Lys1050Asn(p.K1050N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310581 |
| Start | 1255391:1255391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3053A>G |
| AA Mutation | p.Gln1018Arg(p.Q1018R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310581 |
| Start | 1294161:1294161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.725C>T |
| AA Mutation | p.Ala242Val(p.A242V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310581 |
| Start | 1294459:1294459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.427C>T |
| AA Mutation | p.Arg143Cys(p.R143C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310581 |
| Start | 1294566:1294566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.320C>A |
| AA Mutation | p.Ala107Asp(p.A107D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310581 |
| Start | 1272239:1272239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748248614 |
| CDS Mutation | c.2328C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310581 |
| Start | 1294100:1294100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.786G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310581 |
| Start | 1294571:1294571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.315C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310581 |
| Start | 1272197:1272197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376251639 |
| CDS Mutation | c.2370C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310581 |
| Start | 1253764:1253764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750020682 |
| CDS Mutation | c.3363G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310581 |
| Start | 1282506:1282506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377217777 |
| CDS Mutation | c.1692G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310581 |
| Start | 1264496:1264496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375200599 |
| CDS Mutation | c.2751G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310581 |
| Start | 1294783:1294783(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.207delC |
| AA Mutation | p.Ser70ProfsTer8(p.S70Pfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |