Primary Site >> Stomach Cancer
Gene >> MPDZ
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13110650:13110650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5815T>C |
| AA Mutation | p.Ser1939Pro(p.S1939P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13221392:13221392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.856C>A |
| AA Mutation | p.Pro286Thr(p.P286T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13217226:13217226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1155A>C |
| AA Mutation | p.Gln385His(p.Q385H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13150617:13150617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201833535 |
| CDS Mutation | c.3524G>A |
| AA Mutation | p.Arg1175Gln(p.R1175Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13222273:13222273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.707C>T |
| AA Mutation | p.Ser236Phe(p.S236F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13217263:13217263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1118G>T |
| AA Mutation | p.Ser373Ile(p.S373I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13112119:13112119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5629A>G |
| AA Mutation | p.Ile1877Val(p.I1877V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13168392:13168392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3228A>C |
| AA Mutation | p.Arg1076Ser(p.R1076S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13183519:13183519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2548G>A |
| AA Mutation | p.Asp850Asn(p.D850N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13119521:13119521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772107315 |
| CDS Mutation | c.5360C>T |
| AA Mutation | p.Ala1787Val(p.A1787V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13224436:13224436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.331C>T |
| AA Mutation | p.Pro111Ser(p.P111S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13107035:13107035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6143T>C |
| AA Mutation | p.Val2048Ala(p.V2048A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13168519:13168519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376187489 |
| CDS Mutation | c.3101G>A |
| AA Mutation | p.Arg1034Gln(p.R1034Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13247793:13247793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777301563 |
| CDS Mutation | c.25C>T |
| AA Mutation | p.Arg9Trp(p.R9W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13121775:13121775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762930771 |
| CDS Mutation | c.5195C>T |
| AA Mutation | p.Pro1732Leu(p.P1732L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13122133:13122133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4991C>A |
| AA Mutation | p.Ala1664Glu(p.A1664E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13126742:13126742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4495G>A |
| AA Mutation | p.Glu1499Lys(p.E1499K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13136157:13136157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4318G>A |
| AA Mutation | p.Ala1440Thr(p.A1440T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13247748:13247748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759687715 |
| CDS Mutation | c.70C>T |
| AA Mutation | p.Arg24Cys(p.R24C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13222276:13222276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577701969 |
| CDS Mutation | c.704G>A |
| AA Mutation | p.Arg235His(p.R235H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13140139:13140139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3851A>G |
| AA Mutation | p.Gln1284Arg(p.Q1284R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13183510:13183510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2557T>C |
| AA Mutation | p.Tyr853His(p.Y853H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000319217 |
| Start | 13183418:13183418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2649G>T |
| AA Mutation | p.Lys883Asn(p.K883N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13221394:13221394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.854T>A |
| AA Mutation | p.Leu285Gln(p.L285Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13188890:13188890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2258T>C |
| AA Mutation | p.Phe753Ser(p.F753S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13192278:13192278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1821A>T |
| AA Mutation | p.Leu607Phe(p.L607F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319217 |
| Start | 13121755:13121755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5215A>C |
| AA Mutation | p.Ser1739Arg(p.S1739R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000319217 |
| Start | 13219561:13219561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757001915 |
| CDS Mutation | c.1084C>T |
| AA Mutation | p.Arg362Trp(p.R362W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319217 |
| Start | 13168536:13168536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3084C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319217 |
| Start | 13221387:13221387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549732465 |
| CDS Mutation | c.861A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319217 |
| Start | 13190240:13190240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770399719 |
| CDS Mutation | c.2028G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319217 |
| Start | 13143472:13143472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376910378 |
| CDS Mutation | c.3834C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319217 |
| Start | 13107094:13107094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375673261 |
| CDS Mutation | c.6084C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319217 |
| Start | 13188823:13188823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373568505 |
| CDS Mutation | c.2325G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000319217 |
| Start | 13125278:13125278(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4745delA |
| AA Mutation | p.Lys1582ArgfsTer7(p.K1582Rfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000319217 |
| Start | 13110661:13110661(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5804delA |
| AA Mutation | p.Asn1935MetfsTer16(p.N1935Mfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | stop_gained;protein_altering_variant |
| Transcription ID | ENST00000319217 |
| Start | 13150670:13150671(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3470_3471insTAAATAAATAAA |
| AA Mutation | p.Glu1157delinsAspLysTerIleLys(p.E1157delinsDK*IK) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |