Primary Site >> Stomach Cancer
Gene >> TMEM132D
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129084575:129084575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1571T>G |
| AA Mutation | p.Leu524Arg(p.L524R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074345:129074345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2830A>C |
| AA Mutation | p.Lys944Gln(p.K944Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700122:129700122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146143180 |
| CDS Mutation | c.656C>T |
| AA Mutation | p.Pro219Leu(p.P219L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129078709:129078709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1940C>T |
| AA Mutation | p.Ser647Leu(p.S647L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129337644:129337644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1289C>T |
| AA Mutation | p.Pro430Leu(p.P430L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074021:129074021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143281224 |
| CDS Mutation | c.3154G>A |
| AA Mutation | p.Ala1052Thr(p.A1052T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129699925:129699925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757165933 |
| CDS Mutation | c.853C>T |
| AA Mutation | p.Arg285Cys(p.R285C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074519:129074519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2656A>G |
| AA Mutation | p.Thr886Ala(p.T886A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700635:129700635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.143C>T |
| AA Mutation | p.Pro48Leu(p.P48L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129337672:129337672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1261A>T |
| AA Mutation | p.Ser421Cys(p.S421C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129699816:129699816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.962C>T |
| AA Mutation | p.Thr321Met(p.T321M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074830:129074830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746232750 |
| CDS Mutation | c.2345G>A |
| AA Mutation | p.Arg782Gln(p.R782Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129084579:129084579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144267550 |
| CDS Mutation | c.1567C>T |
| AA Mutation | p.Arg523Trp(p.R523W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700142:129700142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.636G>T |
| AA Mutation | p.Arg212Ser(p.R212S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700170:129700170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.608T>C |
| AA Mutation | p.Phe203Ser(p.F203S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700240:129700240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756920052 |
| CDS Mutation | c.538C>T |
| AA Mutation | p.Arg180Trp(p.R180W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074584:129074584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2591A>C |
| AA Mutation | p.Lys864Thr(p.K864T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074552:129074552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2623A>G |
| AA Mutation | p.Asn875Asp(p.N875D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129078687:129078687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1962G>T |
| AA Mutation | p.Lys654Asn(p.K654N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700257:129700257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.521G>A |
| AA Mutation | p.Arg174Gln(p.R174Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129081925:129081925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1757A>C |
| AA Mutation | p.Glu586Ala(p.E586A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129084607:129084607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775382777 |
| CDS Mutation | c.1539C>A |
| AA Mutation | p.Ser513Arg(p.S513R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074027:129074027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755320363 |
| CDS Mutation | c.3148T>C |
| AA Mutation | p.Phe1050Leu(p.F1050L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074156:129074156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3019A>C |
| AA Mutation | p.Asn1007His(p.N1007H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074072:129074072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3103C>T |
| AA Mutation | p.Pro1035Ser(p.P1035S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074581:129074581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2594A>C |
| AA Mutation | p.Lys865Thr(p.K865T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700370:129700370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.408C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129081882:129081882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1800A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129081873:129081873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1809A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074466:129074466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2709G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700687:129700687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.91C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700133:129700133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.645C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700307:129700307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139627769 |
| CDS Mutation | c.471C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074747:129074747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2428A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129074499:129074499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2676G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700196:129700196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774769439 |
| CDS Mutation | c.582C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700207:129700207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.571C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129209652:129209652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1311C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129209532:129209532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1431A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000422113 |
| Start | 129081984:129081984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757029767 |
| CDS Mutation | c.1698C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700160:129700160(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.618delC |
| AA Mutation | p.Thr207ArgfsTer75(p.T207Rfs*75) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000422113 |
| Start | 129074891:129074891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2284G>T |
| AA Mutation | p.Gly762Ter(p.G762*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000422113 |
| Start | 129074056:129074056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3119C>G |
| AA Mutation | p.Ser1040Ter(p.S1040*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700159:129700160(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs747811524 |
| CDS Mutation | c.618dupC |
| AA Mutation | p.Thr207HisfsTer29(p.T207Hfs*29) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000422113 |
| Start | 129700076:129700077(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.701dupG |
| AA Mutation | p.Glu235Ter(p.E235*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |