Primary Site >> Stomach Cancer
Gene >> PXDN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648983:1648983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780009642 |
| CDS Mutation | c.2797C>T |
| AA Mutation | p.Arg933Cys(p.R933C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649600:1649600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748238090 |
| CDS Mutation | c.2180G>A |
| AA Mutation | p.Arg727Gln(p.R727Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648292:1648292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3488G>A |
| AA Mutation | p.Arg1163Gln(p.R1163Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648643:1648643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375863606 |
| CDS Mutation | c.3137C>T |
| AA Mutation | p.Thr1046Met(p.T1046M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648827:1648827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2953A>C |
| AA Mutation | p.Thr985Pro(p.T985P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1666283:1666283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761286747 |
| CDS Mutation | c.1222G>A |
| AA Mutation | p.Gly408Arg(p.G408R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1666426:1666426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746584021 |
| CDS Mutation | c.1079C>T |
| AA Mutation | p.Thr360Met(p.T360M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648679:1648679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3101G>T |
| AA Mutation | p.Trp1034Leu(p.W1034L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1680285:1680285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751455151 |
| CDS Mutation | c.638C>T |
| AA Mutation | p.Ser213Leu(p.S213L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1680291:1680291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187946539 |
| CDS Mutation | c.632C>T |
| AA Mutation | p.Ala211Val(p.A211V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649117:1649117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2663G>A |
| AA Mutation | p.Gly888Asp(p.G888D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648853:1648853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2927A>G |
| AA Mutation | p.His976Arg(p.H976R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1666391:1666391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1114C>T |
| AA Mutation | p.Arg372Trp(p.R372W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1639358:1639358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4017G>T |
| AA Mutation | p.Glu1339Asp(p.E1339D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1666301:1666301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752762698 |
| CDS Mutation | c.1204G>A |
| AA Mutation | p.Val402Ile(p.V402I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649444:1649444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757754304 |
| CDS Mutation | c.2336G>A |
| AA Mutation | p.Arg779Gln(p.R779Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1654502:1654502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs541795687 |
| CDS Mutation | c.1844A>G |
| AA Mutation | p.Asp615Gly(p.D615G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000252804 |
| Start | 1661037:1661037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1681G>A |
| AA Mutation | p.Asp561Asn(p.D561N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648229:1648229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370226454 |
| CDS Mutation | c.3551C>T |
| AA Mutation | p.Thr1184Met(p.T1184M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1666396:1666396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377274038 |
| CDS Mutation | c.1109C>T |
| AA Mutation | p.Pro370Leu(p.P370L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648892:1648892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2888A>G |
| AA Mutation | p.Glu963Gly(p.E963G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649366:1649366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781527729 |
| CDS Mutation | c.2414C>T |
| AA Mutation | p.Thr805Met(p.T805M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649409:1649409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767012980 |
| CDS Mutation | c.2371G>A |
| AA Mutation | p.Ala791Thr(p.A791T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1638923:1638923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4129T>G |
| AA Mutation | p.Ser1377Ala(p.S1377A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1643458:1643458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183629867 |
| CDS Mutation | c.3862G>A |
| AA Mutation | p.Val1288Met(p.V1288M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649582:1649582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372430177 |
| CDS Mutation | c.2198C>T |
| AA Mutation | p.Ser733Leu(p.S733L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648551:1648551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3229G>T |
| AA Mutation | p.Val1077Phe(p.V1077F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1639371:1639371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4004G>C |
| AA Mutation | p.Arg1335Thr(p.R1335T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1643544:1643544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369587687 |
| CDS Mutation | c.3776C>T |
| AA Mutation | p.Pro1259Leu(p.P1259L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649628:1649628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2152G>A |
| AA Mutation | p.Ala718Thr(p.A718T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1639315:1639315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565398993 |
| CDS Mutation | c.4060C>T |
| AA Mutation | p.Arg1354Trp(p.R1354W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1673775:1673775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.886T>G |
| AA Mutation | p.Leu296Val(p.L296V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649108:1649108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2672C>T |
| AA Mutation | p.Ser891Leu(p.S891L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1660914:1660914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1804T>A |
| AA Mutation | p.Ser602Thr(p.S602T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1666288:1666288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1217A>G |
| AA Mutation | p.Asp406Gly(p.D406G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1666342:1666342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778748288 |
| CDS Mutation | c.1163G>A |
| AA Mutation | p.Arg388Gln(p.R388Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649046:1649046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2734G>A |
| AA Mutation | p.Ala912Thr(p.A912T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1643532:1643532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3788C>G |
| AA Mutation | p.Thr1263Ser(p.T1263S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1683719:1683719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.497A>C |
| AA Mutation | p.His166Pro(p.H166P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649178:1649178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2602C>T |
| AA Mutation | p.Arg868Trp(p.R868W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648532:1648532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781648121 |
| CDS Mutation | c.3248G>A |
| AA Mutation | p.Arg1083Gln(p.R1083Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648395:1648395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375850501 |
| CDS Mutation | c.3385C>T |
| AA Mutation | p.Arg1129Cys(p.R1129C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1684115:1684115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.453A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1643501:1643501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3819C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648621:1648621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773257713 |
| CDS Mutation | c.3159C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648786:1648786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2994T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648390:1648390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3390G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648981:1648981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762369823 |
| CDS Mutation | c.2799C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649509:1649509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374573243 |
| CDS Mutation | c.2271C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648909:1648909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2871G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1643516:1643516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752400573 |
| CDS Mutation | c.3804G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648414:1648414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746199083 |
| CDS Mutation | c.3366C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648555:1648555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759679375 |
| CDS Mutation | c.3225G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1666242:1666242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1263C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648591:1648591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369787558 |
| CDS Mutation | c.3189C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1644728:1644728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565581245 |
| CDS Mutation | c.3633C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648234:1648234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3546A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648846:1648846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2934C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648747:1648747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3033C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1635474:1635474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746734526 |
| CDS Mutation | c.4254C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1648441:1648441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3339C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252804 |
| Start | 1649545:1649545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553601622 |
| CDS Mutation | c.2235C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |