Primary Site >> Stomach Cancer
Gene >> PTPRZ1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 121976845:121976845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.613C>T |
| AA Mutation | p.Arg205Cys(p.R205C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122013320:122013320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs62639684 |
| CDS Mutation | c.4274G>A |
| AA Mutation | p.Gly1425Asp(p.G1425D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122055034:122055034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6475C>G |
| AA Mutation | p.Leu2159Val(p.L2159V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122012687:122012687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3641T>G |
| AA Mutation | p.Val1214Gly(p.V1214G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122010850:122010850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1804A>G |
| AA Mutation | p.Asn602Asp(p.N602D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 121968011:121968011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.185C>A |
| AA Mutation | p.Ser62Tyr(p.S62Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122011543:122011543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760236914 |
| CDS Mutation | c.2497C>T |
| AA Mutation | p.Arg833Cys(p.R833C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122013483:122013483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4437G>T |
| AA Mutation | p.Glu1479Asp(p.E1479D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122059868:122059868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6787C>T |
| AA Mutation | p.Pro2263Ser(p.P2263S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122012294:122012294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778883937 |
| CDS Mutation | c.3248C>T |
| AA Mutation | p.Ala1083Val(p.A1083V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122010391:122010391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1345A>C |
| AA Mutation | p.Ser449Arg(p.S449R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 121968077:121968077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.251G>T |
| AA Mutation | p.Gly84Val(p.G84V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122058926:122058926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377355175 |
| CDS Mutation | c.6655A>G |
| AA Mutation | p.Met2219Val(p.M2219V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 121968109:121968109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.283A>C |
| AA Mutation | p.Ile95Leu(p.I95L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 121997934:121997934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1168G>T |
| AA Mutation | p.Ala390Ser(p.A390S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122013050:122013050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4004A>G |
| AA Mutation | p.Glu1335Gly(p.E1335G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122058817:122058817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6546A>C |
| AA Mutation | p.Glu2182Asp(p.E2182D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122011964:122011964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2918A>C |
| AA Mutation | p.Lys973Thr(p.K973T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122039488:122039488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5537G>T |
| AA Mutation | p.Ser1846Ile(p.S1846I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122011364:122011364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2318C>A |
| AA Mutation | p.Pro773His(p.P773H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122010452:122010452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs185158958 |
| CDS Mutation | c.1406G>A |
| AA Mutation | p.Arg469His(p.R469H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122013563:122013563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4517C>T |
| AA Mutation | p.Pro1506Leu(p.P1506L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122058852:122058852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6581C>T |
| AA Mutation | p.Pro2194Leu(p.P2194L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122013335:122013335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4289A>G |
| AA Mutation | p.Asp1430Gly(p.D1430G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122012911:122012911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3865A>G |
| AA Mutation | p.Asn1289Asp(p.N1289D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122019226:122019226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4946T>G |
| AA Mutation | p.Phe1649Cys(p.F1649C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122038875:122038875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150233853 |
| CDS Mutation | c.5488G>A |
| AA Mutation | p.Val1830Met(p.V1830M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122044494:122044494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753904600 |
| CDS Mutation | c.6010C>T |
| AA Mutation | p.His2004Tyr(p.H2004Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000393386 |
| Start | 122039455:122039455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5504G>T |
| AA Mutation | p.Arg1835Ile(p.R1835I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122010376:122010376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1330A>G |
| AA Mutation | p.Asn444Asp(p.N444D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000393386 |
| Start | 122039572:122039572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5621A>C |
| AA Mutation | p.Asn1874Thr(p.N1874T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122011917:122011917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2871T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122012565:122012565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3519A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122012463:122012463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761365256 |
| CDS Mutation | c.3417G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122013630:122013630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4584T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122013588:122013588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778135169 |
| CDS Mutation | c.4542G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122011728:122011728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2682T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122012583:122012583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3537A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122010603:122010603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1557T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122011083:122011083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2037T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122011593:122011593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147331896 |
| CDS Mutation | c.2547C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122039568:122039568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5617A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 121983732:121983732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.687C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000393386 |
| Start | 122010948:122010948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201117894 |
| CDS Mutation | c.1902A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |