Primary Site >> Stomach Cancer
Gene >> TRIM37
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000262294 |
| Start | 59091340:59091340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.124C>T |
| AA Mutation | p.Arg42Cys(p.R42C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262294 |
| Start | 59012407:59012407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2616G>A |
| AA Mutation | p.Met872Ile(p.M872I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262294 |
| Start | 59088373:59088373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781030263 |
| CDS Mutation | c.199C>T |
| AA Mutation | p.Arg67Cys(p.R67C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262294 |
| Start | 59049296:59049296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764519568 |
| CDS Mutation | c.1412G>A |
| AA Mutation | p.Arg471Gln(p.R471Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262294 |
| Start | 59047698:59047698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1652T>C |
| AA Mutation | p.Ile551Thr(p.I551T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262294 |
| Start | 59079816:59079816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.554C>T |
| AA Mutation | p.Ala185Val(p.A185V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262294 |
| Start | 59015647:59015647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2539C>T |
| AA Mutation | p.Pro847Ser(p.P847S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262294 |
| Start | 59104387:59104387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779987594 |
| CDS Mutation | c.29C>T |
| AA Mutation | p.Ala10Val(p.A10V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262294 |
| Start | 59057009:59057009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1065T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262294 |
| Start | 59031915:59031915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1929T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262294 |
| Start | 59081157:59081157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.432T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262294 |
| Start | 59057001:59057001(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1073delA |
| AA Mutation | p.Asn358IlefsTer33(p.N358Ifs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262294 |
| Start | 59031994:59032003(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1841_1850delTTGATCCATT |
| AA Mutation | p.Ile614LysfsTer3(p.I614Kfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000262294 |
| Start | 59049297:59049297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs386834001 |
| CDS Mutation | c.1411C>T |
| AA Mutation | p.Arg471Ter(p.R471*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |