Primary Site >> Stomach Cancer
Gene >> SV2A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149910937:149910937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.844G>C |
| AA Mutation | p.Glu282Gln(p.E282Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149908055:149908055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1531T>C |
| AA Mutation | p.Tyr511His(p.Y511H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149906725:149906725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1810G>A |
| AA Mutation | p.Gly604Arg(p.G604R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149909252:149909252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1319G>A |
| AA Mutation | p.Gly440Asp(p.G440D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149913295:149913295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.546G>T |
| AA Mutation | p.Glu182Asp(p.E182D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149910883:149910883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.898T>C |
| AA Mutation | p.Trp300Arg(p.W300R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149913534:149913534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144624887 |
| CDS Mutation | c.307C>T |
| AA Mutation | p.Arg103Trp(p.R103W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149909519:149909519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372487028 |
| CDS Mutation | c.1232C>T |
| AA Mutation | p.Ser411Leu(p.S411L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149911911:149911911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.692G>A |
| AA Mutation | p.Arg231Gln(p.R231Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149911943:149911943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.660C>A |
| AA Mutation | p.Phe220Leu(p.F220L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149913435:149913435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782452680 |
| CDS Mutation | c.406C>T |
| AA Mutation | p.Arg136Trp(p.R136W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149913705:149913705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781932183 |
| CDS Mutation | c.136T>C |
| AA Mutation | p.Tyr46His(p.Y46H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149910862:149910862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.919G>A |
| AA Mutation | p.Ala307Thr(p.A307T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369146 |
| Start | 149907739:149907739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200597235 |
| CDS Mutation | c.1639C>T |
| AA Mutation | p.Arg547Cys(p.R547C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369146 |
| Start | 149913436:149913436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.405C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369146 |
| Start | 149913304:149913304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781860737 |
| CDS Mutation | c.537C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369146 |
| Start | 149910651:149910651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369666694 |
| CDS Mutation | c.1008C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369146 |
| Start | 149909248:149909248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1323C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369146 |
| Start | 149913429:149913429(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.412delG |
| AA Mutation | p.Glu138ArgfsTer39(p.E138Rfs*39) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369146 |
| Start | 149913467:149913467(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.374delG |
| AA Mutation | p.Gly125AlafsTer2(p.G125Afs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000369146 |
| Start | 149910916:149910916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782707236 |
| CDS Mutation | c.865C>T |
| AA Mutation | p.Arg289Ter(p.R289*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |