Primary Site >> Stomach Cancer
Gene >> CRIM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36512301:36512301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1687C>T |
| AA Mutation | p.Arg563Cys(p.R563C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36544434:36544434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2682G>T |
| AA Mutation | p.Glu894Asp(p.E894D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36544401:36544401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2649T>G |
| AA Mutation | p.Asn883Lys(p.N883K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36517517:36517517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2181G>T |
| AA Mutation | p.Gln727His(p.Q727H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36522103:36522103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764343849 |
| CDS Mutation | c.2218C>T |
| AA Mutation | p.Arg740Trp(p.R740W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36537403:36537403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2480C>T |
| AA Mutation | p.Ala827Val(p.A827V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36479637:36479637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746293769 |
| CDS Mutation | c.1315G>A |
| AA Mutation | p.Gly439Arg(p.G439R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36544480:36544480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2728A>G |
| AA Mutation | p.Ile910Val(p.I910V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36441407:36441407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.655C>T |
| AA Mutation | p.Arg219Cys(p.R219C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36464643:36464643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.979G>C |
| AA Mutation | p.Glu327Gln(p.E327Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36441423:36441423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767692280 |
| CDS Mutation | c.671C>T |
| AA Mutation | p.Pro224Leu(p.P224L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36476988:36476988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1091C>T |
| AA Mutation | p.Ala364Val(p.A364V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000280527 |
| Start | 36512370:36512370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755928305 |
| CDS Mutation | c.1756G>A |
| AA Mutation | p.Gly586Ser(p.G586S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280527 |
| Start | 36522195:36522195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769119378 |
| CDS Mutation | c.2310C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280527 |
| Start | 36356439:36356439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.147G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280527 |
| Start | 36513693:36513693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1918C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280527 |
| Start | 36513623:36513623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1848T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280527 |
| Start | 36476983:36476983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1086C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000280527 |
| Start | 36522225:36522225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142923562 |
| CDS Mutation | c.2340C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000280527 |
| Start | 36522266:36522266(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2381delG |
| AA Mutation | p.Cys794LeufsTer6(p.C794Lfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |