Primary Site >> Stomach Cancer
Gene >> RP1L1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612831:10612831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375440665 |
| CDS Mutation | c.1267C>T |
| AA Mutation | p.Arg423Trp(p.R423W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10611696:10611696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2402A>G |
| AA Mutation | p.Gln801Arg(p.Q801R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10611905:10611905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2193C>A |
| AA Mutation | p.Asp731Glu(p.D731E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10609041:10609041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751906682 |
| CDS Mutation | c.5057C>T |
| AA Mutation | p.Ala1686Val(p.A1686V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10607685:10607685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6413A>G |
| AA Mutation | p.Glu2138Gly(p.E2138G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612801:10612801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199589914 |
| CDS Mutation | c.1297C>T |
| AA Mutation | p.Arg433Cys(p.R433C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10607813:10607813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6285G>T |
| AA Mutation | p.Gln2095His(p.Q2095H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612095:10612095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2003C>T |
| AA Mutation | p.Ser668Phe(p.S668F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10622825:10622825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.377C>A |
| AA Mutation | p.Ala126Asp(p.A126D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10623015:10623015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368569447 |
| CDS Mutation | c.187G>A |
| AA Mutation | p.Ala63Thr(p.A63T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10607206:10607206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6892C>T |
| AA Mutation | p.Pro2298Ser(p.P2298S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10611880:10611880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2218G>A |
| AA Mutation | p.Val740Ile(p.V740I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612964:10612964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1134G>T |
| AA Mutation | p.Glu378Asp(p.E378D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10610416:10610416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3682A>G |
| AA Mutation | p.Thr1228Ala(p.T1228A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10610932:10610932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3166G>A |
| AA Mutation | p.Ala1056Thr(p.A1056T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10622798:10622798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.404A>G |
| AA Mutation | p.Gln135Arg(p.Q135R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10607557:10607557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6541G>C |
| AA Mutation | p.Glu2181Gln(p.E2181Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10608706:10608706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5392A>C |
| AA Mutation | p.Ser1798Arg(p.S1798R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10606954:10606954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776156711 |
| CDS Mutation | c.7144G>A |
| AA Mutation | p.Ala2382Thr(p.A2382T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10610800:10610800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201017740 |
| CDS Mutation | c.3298G>A |
| AA Mutation | p.Val1100Met(p.V1100M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10610703:10610703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3395T>C |
| AA Mutation | p.Leu1132Pro(p.L1132P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10607665:10607665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6433T>C |
| AA Mutation | p.Ser2145Pro(p.S2145P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612735:10612735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1363C>T |
| AA Mutation | p.Pro455Ser(p.P455S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612446:10612446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758393932 |
| CDS Mutation | c.1652G>A |
| AA Mutation | p.Arg551Gln(p.R551Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10609521:10609521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267601688 |
| CDS Mutation | c.4577C>T |
| AA Mutation | p.Thr1526Met(p.T1526M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10610838:10610838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3260G>A |
| AA Mutation | p.Arg1087Lys(p.R1087K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10610024:10610024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4074A>C |
| AA Mutation | p.Glu1358Asp(p.E1358D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612213:10612213(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1885T>C |
| AA Mutation | p.Ser629Pro(p.S629P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10607035:10607035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs185197824 |
| CDS Mutation | c.7063G>A |
| AA Mutation | p.Ala2355Thr(p.A2355T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382483 |
| Start | 10622748:10622748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.454C>T |
| AA Mutation | p.Arg152Trp(p.R152W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10608920:10608920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5178T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10610237:10610237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775461512 |
| CDS Mutation | c.3861G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612814:10612814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1284G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10623004:10623004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148800956 |
| CDS Mutation | c.198C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10609223:10609223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4875C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10613006:10613006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1092C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10608929:10608929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5169C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10610711:10610711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3387G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612115:10612115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199628229 |
| CDS Mutation | c.1983G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10613090:10613090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764660293 |
| CDS Mutation | c.1008G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10610612:10610612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112361777 |
| CDS Mutation | c.3486C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10616468:10616468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.729G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10608590:10608590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5508G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10607123:10607123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6975C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10608446:10608446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372030347 |
| CDS Mutation | c.5652G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10613306:10613306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs567914782 |
| CDS Mutation | c.792G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10609193:10609193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200540100 |
| CDS Mutation | c.4905C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10611224:10611224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749489002 |
| CDS Mutation | c.2874C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10623052:10623052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.150C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10609787:10609787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4311C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612409:10612409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1689C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382483 |
| Start | 10613102:10613102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs562466295 |
| CDS Mutation | c.996C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382483 |
| Start | 10612950:10612950(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1148delG |
| AA Mutation | p.Gly383AspfsTer107(p.G383Dfs*107) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382483 |
| Start | 10613247:10613247(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.851delC |
| AA Mutation | p.Pro284ArgfsTer26(p.P284Rfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382483 |
| Start | 10622872:10622872(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.330delC |
| AA Mutation | p.Lys111ArgfsTer46(p.K111Rfs*46) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000382483 |
| Start | 10607965:10607965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6133G>T |
| AA Mutation | p.Glu2045Ter(p.E2045*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000382483 |
| Start | 10611991:10611991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775708703 |
| CDS Mutation | c.2107C>T |
| AA Mutation | p.Arg703Ter(p.R703*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000382483 |
| Start | 10609612:10609613(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.4485dupC |
| AA Mutation | p.Thr1496HisfsTer45(p.T1496Hfs*45) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000382483 |
| Start | 10608098:10608099(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.5999_6000insTTTTTCCCCCTGCGTTGCGTC |
| AA Mutation | p.Val2000_Glu2001insPheSerProCysValAlaSer(p.V2000_E2001insFSPCVAS) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |