Primary Site >> Stomach Cancer
Gene >> MKRN3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566492:23566492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.710T>C |
| AA Mutation | p.Val237Ala(p.V237A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23567091:23567091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1309T>C |
| AA Mutation | p.Ser437Pro(p.S437P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566723:23566723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.941G>T |
| AA Mutation | p.Cys314Phe(p.C314F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566038:23566038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.256C>A |
| AA Mutation | p.Pro86Thr(p.P86T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566764:23566764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.982C>T |
| AA Mutation | p.Arg328Cys(p.R328C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23567150:23567150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1368G>T |
| AA Mutation | p.Met456Ile(p.M456I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566942:23566942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1160T>G |
| AA Mutation | p.Leu387Arg(p.L387R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566604:23566604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.822G>C |
| AA Mutation | p.Leu274Phe(p.L274F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566152:23566152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202089304 |
| CDS Mutation | c.370C>T |
| AA Mutation | p.Arg124Trp(p.R124W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23565874:23565874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.92A>C |
| AA Mutation | p.Asp31Ala(p.D31A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566051:23566051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140349866 |
| CDS Mutation | c.269G>A |
| AA Mutation | p.Arg90Gln(p.R90Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566815:23566815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373441581 |
| CDS Mutation | c.1033C>T |
| AA Mutation | p.Arg345Cys(p.R345C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23567211:23567211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767507343 |
| CDS Mutation | c.1429C>T |
| AA Mutation | p.Arg477Trp(p.R477W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566559:23566559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.777G>A |
| AA Mutation | p.Met259Ile(p.M259I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566858:23566858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769287405 |
| CDS Mutation | c.1076A>C |
| AA Mutation | p.Lys359Thr(p.K359T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566563:23566563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.781C>A |
| AA Mutation | p.Leu261Ile(p.L261I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566153:23566153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200032750 |
| CDS Mutation | c.371G>A |
| AA Mutation | p.Arg124Gln(p.R124Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566726:23566726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.944T>C |
| AA Mutation | p.Met315Thr(p.M315T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566719:23566719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.937A>T |
| AA Mutation | p.Ile313Phe(p.I313F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23567088:23567088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1306G>T |
| AA Mutation | p.Gly436Trp(p.G436W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566919:23566919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1137G>T |
| AA Mutation | p.Glu379Asp(p.E379D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566301:23566301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774367502 |
| CDS Mutation | c.519G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314520 |
| Start | 23567105:23567105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1323C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566682:23566682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.900G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566229:23566229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569949058 |
| CDS Mutation | c.447C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566258:23566258(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.482delC |
| AA Mutation | p.Pro161ArgfsTer10(p.P161Rfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000314520 |
| Start | 23566257:23566258(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs763195944 |
| CDS Mutation | c.482dupC |
| AA Mutation | p.Ala162GlyfsTer15(p.A162Gfs*15) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |