Primary Site >> Stomach Cancer
Gene >> GSE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85661643:85661643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2138G>A |
| AA Mutation | p.Arg713Gln(p.R713Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85663013:85663013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753550740 |
| CDS Mutation | c.2293G>A |
| AA Mutation | p.Glu765Lys(p.E765K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85655842:85655842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199912131 |
| CDS Mutation | c.914G>A |
| AA Mutation | p.Arg305His(p.R305H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85657303:85657303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1339G>A |
| AA Mutation | p.Ala447Thr(p.A447T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85668251:85668251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3242G>T |
| AA Mutation | p.Gly1081Val(p.G1081V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85671010:85671010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3431G>T |
| AA Mutation | p.Arg1144Leu(p.R1144L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85661484:85661484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1979G>A |
| AA Mutation | p.Gly660Glu(p.G660E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85654441:85654441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199764093 |
| CDS Mutation | c.590C>T |
| AA Mutation | p.Pro197Leu(p.P197L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85663377:85663377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2407A>G |
| AA Mutation | p.Thr803Ala(p.T803A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85666237:85666237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3020G>A |
| AA Mutation | p.Ser1007Asn(p.S1007N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85654834:85654834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773762744 |
| CDS Mutation | c.640G>A |
| AA Mutation | p.Val214Met(p.V214M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85657288:85657288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1324G>A |
| AA Mutation | p.Asp442Asn(p.D442N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85634015:85634015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.109G>A |
| AA Mutation | p.Ala37Thr(p.A37T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85663064:85663064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2344C>T |
| AA Mutation | p.Pro782Ser(p.P782S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85668145:85668145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766062436 |
| CDS Mutation | c.3136G>A |
| AA Mutation | p.Val1046Met(p.V1046M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85655868:85655868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.940T>G |
| AA Mutation | p.Ser314Ala(p.S314A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85654847:85654847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.653A>G |
| AA Mutation | p.Tyr218Cys(p.Y218C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253458 |
| Start | 85657556:85657556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769714454 |
| CDS Mutation | c.1592G>A |
| AA Mutation | p.Arg531Gln(p.R531Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253458 |
| Start | 85668228:85668228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756601856 |
| CDS Mutation | c.3219C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253458 |
| Start | 85668144:85668144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3135C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253458 |
| Start | 85655912:85655912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376374898 |
| CDS Mutation | c.984G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000253458 |
| Start | 85661181:85661187(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1676_1682delACCCTCC |
| AA Mutation | p.Asp559GlyfsTer10(p.D559Gfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000253458 |
| Start | 85657484:85657486(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1522_1524delAAG |
| AA Mutation | p.Lys508del(p.K508del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |