Primary Site >> Stomach Cancer
Gene >> SAGE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135901596:135901596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.125G>A |
| AA Mutation | p.Gly42Glu(p.G42E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135910044:135910044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1738C>A |
| AA Mutation | p.His580Asn(p.H580N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135906989:135906989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.800A>C |
| AA Mutation | p.Asn267Thr(p.N267T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135911683:135911683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2251A>G |
| AA Mutation | p.Thr751Ala(p.T751A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135911234:135911234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2048A>C |
| AA Mutation | p.Asn683Thr(p.N683T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135911749:135911749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2317G>C |
| AA Mutation | p.Asp773His(p.D773H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135907430:135907430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367622228 |
| CDS Mutation | c.995C>T |
| AA Mutation | p.Pro332Leu(p.P332L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135907364:135907364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782012489 |
| CDS Mutation | c.929C>T |
| AA Mutation | p.Pro310Leu(p.P310L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135908485:135908485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782285077 |
| CDS Mutation | c.1309G>A |
| AA Mutation | p.Val437Ile(p.V437I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135911670:135911670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2238G>T |
| AA Mutation | p.Glu746Asp(p.E746D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135901622:135901622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.151A>G |
| AA Mutation | p.Arg51Gly(p.R51G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135905329:135905329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.391G>A |
| AA Mutation | p.Ala131Thr(p.A131T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324447 |
| Start | 135908947:135908947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1525C>A |
| AA Mutation | p.Pro509Thr(p.P509T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324447 |
| Start | 135908931:135908931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1509C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324447 |
| Start | 135904514:135904514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.258A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_retained_variant |
| Transcription ID | ENST00000324447 |
| Start | 135912897:135912897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2715A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324447 |
| Start | 135907431:135907431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.996G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324447 |
| Start | 135904487:135904487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.231C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324447 |
| Start | 135912802:135912802(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2625delA |
| AA Mutation | p.Val876LeufsTer3(p.V876Lfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324447 |
| Start | 135911895:135911895(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2463delG |
| AA Mutation | p.Ile823LeufsTer5(p.I823Lfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324447 |
| Start | 135906450:135906450(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.638delA |
| AA Mutation | p.Asn213MetfsTer11(p.N213Mfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000324447 |
| Start | 135911938:135911938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782625354 |
| CDS Mutation | c.2506C>T |
| AA Mutation | p.Arg836Ter(p.R836*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000324447 |
| Start | 135911891:135911892(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2462dupA |
| AA Mutation | p.Lys822GlufsTer3(p.K822Efs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |