Primary Site >> Stomach Cancer
Gene >> PDS5B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32699855:32699855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1726G>A |
| AA Mutation | p.Ala576Thr(p.A576T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32651944:32651944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.249C>G |
| AA Mutation | p.Cys83Trp(p.C83W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32701333:32701333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1751C>G |
| AA Mutation | p.Thr584Ser(p.T584S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32773193:32773193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4177G>A |
| AA Mutation | p.Val1393Ile(p.V1393I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32701432:32701432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1850C>A |
| AA Mutation | p.Ser617Tyr(p.S617Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32706974:32706974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1897G>A |
| AA Mutation | p.Ala633Thr(p.A633T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32687143:32687143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1213C>T |
| AA Mutation | p.Arg405Cys(p.R405C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32688494:32688494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1394C>A |
| AA Mutation | p.Pro465His(p.P465H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315596 |
| Start | 32732207:32732207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2230T>C |
| AA Mutation | p.Phe744Leu(p.F744L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000315596 |
| Start | 32770560:32770560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4064G>T |
| AA Mutation | p.Arg1355Ile(p.R1355I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315596 |
| Start | 32735291:32735291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2367A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315596 |
| Start | 32770696:32770696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4107C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315596 |
| Start | 32764531:32764531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3561C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315596 |
| Start | 32770480:32770480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3984A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315596 |
| Start | 32732176:32732176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2199C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315596 |
| Start | 32648793:32648793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.21G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315596 |
| Start | 32770430:32770430(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3939delA |
| AA Mutation | p.Gly1314GlufsTer80(p.G1314Efs*80) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315596 |
| Start | 32651893:32651893(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.204delT |
| AA Mutation | p.Leu69SerfsTer12(p.L69Sfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315596 |
| Start | 32770750:32770751(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4168_4169delAA |
| AA Mutation | p.Asn1390CysfsTer12(p.N1390Cfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315596 |
| Start | 32764556:32764556(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs755801132 |
| CDS Mutation | c.3592delA |
| AA Mutation | p.Ser1198ValfsTer10(p.S1198Vfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315596 |
| Start | 32770148:32770148(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3658delA |
| AA Mutation | p.Thr1220ArgfsTer10(p.T1220Rfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315596 |
| Start | 32770750:32770750(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs759495724 |
| CDS Mutation | c.4169delA |
| AA Mutation | p.Asn1390MetfsTer4(p.N1390Mfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315596 |
| Start | 32732141:32732141(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2170delC |
| AA Mutation | p.Arg724ValfsTer32(p.R724Vfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315596 |
| Start | 32683955:32683955(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1139delA |
| AA Mutation | p.Lys380ArgfsTer14(p.K380Rfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315596 |
| Start | 32741089:32741089(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2420delA |
| AA Mutation | p.Lys807ArgfsTer25(p.K807Rfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000315596 |
| Start | 32684000:32684000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750827034 |
| CDS Mutation | c.1180A>T |
| AA Mutation | p.Arg394Ter(p.R394*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000315596 |
| Start | 32651846:32651846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.151G>T |
| AA Mutation | p.Glu51Ter(p.E51*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |