Primary Site >> Stomach Cancer
Gene >> ADAMTS5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26966046:26966046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773798738 |
| CDS Mutation | c.346G>A |
| AA Mutation | p.Ala116Thr(p.A116T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26924317:26924317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2529A>T |
| AA Mutation | p.Leu843Phe(p.L843F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26924310:26924310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371425346 |
| CDS Mutation | c.2536C>T |
| AA Mutation | p.Arg846Cys(p.R846C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26930028:26930028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2083A>C |
| AA Mutation | p.Asn695His(p.N695H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26965551:26965551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766100243 |
| CDS Mutation | c.841C>T |
| AA Mutation | p.Arg281Trp(p.R281W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26965670:26965670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.722A>T |
| AA Mutation | p.Gln241Leu(p.Q241L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26954745:26954745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1231G>A |
| AA Mutation | p.Glu411Lys(p.E411K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26934559:26934559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1596G>C |
| AA Mutation | p.Lys532Asn(p.K532N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26934499:26934499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1656A>T |
| AA Mutation | p.Lys552Asn(p.K552N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26966117:26966117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.275A>G |
| AA Mutation | p.Tyr92Cys(p.Y92C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26965746:26965746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.646C>T |
| AA Mutation | p.Pro216Ser(p.P216S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26966222:26966222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.170C>A |
| AA Mutation | p.Pro57His(p.P57H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26954840:26954840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1136T>C |
| AA Mutation | p.Leu379Pro(p.L379P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26965731:26965731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.661C>T |
| AA Mutation | p.His221Tyr(p.H221Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26934686:26934686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1469C>T |
| AA Mutation | p.Thr490Ile(p.T490I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26934588:26934588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759375195 |
| CDS Mutation | c.1567C>T |
| AA Mutation | p.Arg523Cys(p.R523C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26932032:26932032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2021C>T |
| AA Mutation | p.Thr674Ile(p.T674I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26965910:26965910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.482C>T |
| AA Mutation | p.Ala161Val(p.A161V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26965773:26965773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.619G>A |
| AA Mutation | p.Ala207Thr(p.A207T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26924123:26924123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2723A>C |
| AA Mutation | p.Lys908Thr(p.K908T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26943483:26943483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1302A>C |
| AA Mutation | p.Glu434Asp(p.E434D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26924486:26924486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2360A>T |
| AA Mutation | p.Asn787Ile(p.N787I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26965358:26965358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1034A>C |
| AA Mutation | p.Gln345Pro(p.Q345P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26934627:26934627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368628024 |
| CDS Mutation | c.1528G>A |
| AA Mutation | p.Gly510Ser(p.G510S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26934556:26934556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1599G>T |
| AA Mutation | p.Lys533Asn(p.K533N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26934633:26934633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1522T>C |
| AA Mutation | p.Cys508Arg(p.C508R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26933006:26933006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1728G>T |
| AA Mutation | p.Trp576Cys(p.W576C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000284987 |
| Start | 26954869:26954869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1107T>G |
| AA Mutation | p.Asp369Glu(p.D369E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26932068:26932068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768917351 |
| CDS Mutation | c.1985C>T |
| AA Mutation | p.Ala662Val(p.A662V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26966012:26966012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.380G>A |
| AA Mutation | p.Arg127Gln(p.R127Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26943481:26943481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1304A>G |
| AA Mutation | p.Asp435Gly(p.D435G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26965805:26965805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.587A>G |
| AA Mutation | p.Glu196Gly(p.E196G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26966261:26966261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.131G>A |
| AA Mutation | p.Arg44His(p.R44H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26965916:26965916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.476A>C |
| AA Mutation | p.Lys159Thr(p.K159T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284987 |
| Start | 26924222:26924222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753190231 |
| CDS Mutation | c.2624C>T |
| AA Mutation | p.Ser875Leu(p.S875L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26966110:26966110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.282C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26954857:26954857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1119T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26924368:26924368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373445194 |
| CDS Mutation | c.2478G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26924215:26924215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764765778 |
| CDS Mutation | c.2631G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26930023:26930023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763923215 |
| CDS Mutation | c.2088C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26924521:26924521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2325A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26924518:26924518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2328C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26965552:26965552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.840G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26966094:26966094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.298T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26933021:26933021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1713A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284987 |
| Start | 26934535:26934535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199797191 |
| CDS Mutation | c.1620G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |