Primary Site >> Stomach Cancer
Gene >> SBF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 10000924:10000924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.851T>A |
| AA Mutation | p.Val284Asp(p.V284D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 10029851:10029851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142469360 |
| CDS Mutation | c.427G>A |
| AA Mutation | p.Val143Met(p.V143M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 10193976:10193976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571646224 |
| CDS Mutation | c.67G>T |
| AA Mutation | p.Gly23Cys(p.G23C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 10002603:10002603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.706G>A |
| AA Mutation | p.Asp236Asn(p.D236N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9853569:9853569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2507A>G |
| AA Mutation | p.His836Arg(p.H836R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9780448:9780448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5520C>A |
| AA Mutation | p.Asp1840Glu(p.D1840E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9789141:9789141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4900A>G |
| AA Mutation | p.Thr1634Ala(p.T1634A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9839502:9839502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140550985 |
| CDS Mutation | c.3451C>T |
| AA Mutation | p.Arg1151Trp(p.R1151W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9858264:9858264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2062G>T |
| AA Mutation | p.Ala688Ser(p.A688S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9968395:9968395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1546C>G |
| AA Mutation | p.Pro516Ala(p.P516A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9789122:9789122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4919C>T |
| AA Mutation | p.Thr1640Ile(p.T1640I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9850041:9850041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2788A>G |
| AA Mutation | p.Thr930Ala(p.T930A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9856708:9856708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2113G>T |
| AA Mutation | p.Asp705Tyr(p.D705Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9856657:9856657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753111342 |
| CDS Mutation | c.2164C>T |
| AA Mutation | p.Arg722Cys(p.R722C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9853707:9853707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2369C>T |
| AA Mutation | p.Ala790Val(p.A790V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9781566:9781566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5392A>G |
| AA Mutation | p.Ile1798Val(p.I1798V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256190 |
| Start | 9817007:9817007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765001700 |
| CDS Mutation | c.3811C>T |
| AA Mutation | p.Arg1271Cys(p.R1271C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256190 |
| Start | 9832393:9832393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770660788 |
| CDS Mutation | c.3483A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256190 |
| Start | 9839650:9839650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531651423 |
| CDS Mutation | c.3303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |