Primary Site >> Stomach Cancer
Gene >> SEMA3F
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50174092:50174092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.314T>C |
| AA Mutation | p.Val105Ala(p.V105A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50186016:50186016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1715C>T |
| AA Mutation | p.Ala572Val(p.A572V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50182683:50182683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803C>T |
| AA Mutation | p.Ala268Val(p.A268V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50184664:50184664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1306C>T |
| AA Mutation | p.Arg436Cys(p.R436C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50183554:50183554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137935899 |
| CDS Mutation | c.1223G>A |
| AA Mutation | p.Arg408Gln(p.R408Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50182962:50182962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962G>A |
| AA Mutation | p.Arg321Gln(p.R321Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50186742:50186742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780169693 |
| CDS Mutation | c.1943G>A |
| AA Mutation | p.Arg648Gln(p.R648Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50185448:50185448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749098669 |
| CDS Mutation | c.1462G>A |
| AA Mutation | p.Gly488Arg(p.G488R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50174077:50174077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554250122 |
| CDS Mutation | c.299G>A |
| AA Mutation | p.Arg100His(p.R100H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50175162:50175162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372800240 |
| CDS Mutation | c.523C>T |
| AA Mutation | p.Arg175Cys(p.R175C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50159704:50159704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.82G>A |
| AA Mutation | p.Ala28Thr(p.A28T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000002829 |
| Start | 50173834:50173834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.154C>T |
| AA Mutation | p.Leu52Phe(p.L52F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000002829 |
| Start | 50173908:50173908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757048607 |
| CDS Mutation | c.228C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000002829 |
| Start | 50182327:50182327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764044538 |
| CDS Mutation | c.687T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000002829 |
| Start | 50187938:50187938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2181C>A |
| AA Mutation | p.Tyr727Ter(p.Y727*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |