Primary Site >> Stomach Cancer
Gene >> POP1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000349693 |
| Start | 98156051:98156051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142902409 |
| CDS Mutation | c.2059C>T |
| AA Mutation | p.Arg687Cys(p.R687C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98134511:98134511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144135573 |
| CDS Mutation | c.863G>A |
| AA Mutation | p.Arg288His(p.R288H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98127685:98127685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.233A>G |
| AA Mutation | p.Lys78Arg(p.K78R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98158023:98158023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2827C>A |
| AA Mutation | p.Leu943Met(p.L943M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98134619:98134619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.971G>A |
| AA Mutation | p.Ser324Asn(p.S324N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98123427:98123427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.90A>T |
| AA Mutation | p.Arg30Ser(p.R30S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98127744:98127744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.292A>C |
| AA Mutation | p.Ile98Leu(p.I98L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98128415:98128415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.361G>A |
| AA Mutation | p.Ala121Thr(p.A121T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98134535:98134535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371524249 |
| CDS Mutation | c.887G>A |
| AA Mutation | p.Arg296Gln(p.R296Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98136532:98136532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1062A>C |
| AA Mutation | p.Lys354Asn(p.K354N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98156255:98156255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2263C>T |
| AA Mutation | p.Pro755Ser(p.P755S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98156322:98156322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2330G>A |
| AA Mutation | p.Cys777Tyr(p.C777Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98130122:98130122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.631C>T |
| AA Mutation | p.Arg211Trp(p.R211W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98127709:98127709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.257G>A |
| AA Mutation | p.Gly86Glu(p.G86E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98157837:98157837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2641G>A |
| AA Mutation | p.Glu881Lys(p.E881K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98156106:98156106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2114G>A |
| AA Mutation | p.Cys705Tyr(p.C705Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349693 |
| Start | 98156297:98156297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2305G>A |
| AA Mutation | p.Ala769Thr(p.A769T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349693 |
| Start | 98157803:98157803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772916913 |
| CDS Mutation | c.2607C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349693 |
| Start | 98158004:98158004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146111575 |
| CDS Mutation | c.2808C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349693 |
| Start | 98156191:98156191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764185469 |
| CDS Mutation | c.2199T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349693 |
| Start | 98136891:98136891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1299G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000349693 |
| Start | 98156240:98156240(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2254delA |
| AA Mutation | p.Thr752LeufsTer12(p.T752Lfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000349693 |
| Start | 98136659:98136659(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1195delA |
| AA Mutation | p.Ile399LeufsTer23(p.I399Lfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000349693 |
| Start | 98150635:98150635(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2056delA |
| AA Mutation | p.Arg686AspfsTer26(p.R686Dfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000349693 |
| Start | 98146585:98146585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770043633 |
| CDS Mutation | c.1612C>T |
| AA Mutation | p.Gln538Ter(p.Q538*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000349693 |
| Start | 98127708:98127708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150709391 |
| CDS Mutation | c.256G>T |
| AA Mutation | p.Gly86Ter(p.G86*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |