Primary Site >> Stomach Cancer
Gene >> DIAPH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141528754:141528754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2966C>T |
| AA Mutation | p.Ala989Val(p.A989V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141528773:141528773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2947G>A |
| AA Mutation | p.Val983Ile(p.V983I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141516966:141516966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761387295 |
| CDS Mutation | c.3704C>T |
| AA Mutation | p.Ser1235Leu(p.S1235L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141571985:141571985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752824698 |
| CDS Mutation | c.2414G>A |
| AA Mutation | p.Arg805His(p.R805H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141528841:141528841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2879T>C |
| AA Mutation | p.Val960Ala(p.V960A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141575097:141575097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1511A>C |
| AA Mutation | p.Lys504Thr(p.K504T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141571962:141571962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147203145 |
| CDS Mutation | c.2437G>A |
| AA Mutation | p.Ala813Thr(p.A813T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141578541:141578541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1018C>T |
| AA Mutation | p.Arg340Cys(p.R340C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141516988:141516988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3682G>A |
| AA Mutation | p.Ala1228Thr(p.A1228T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141526434:141526434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3301T>C |
| AA Mutation | p.Tyr1101His(p.Y1101H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389054 |
| Start | 141528819:141528819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2901A>C |
| AA Mutation | p.Leu967Phe(p.L967F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389054 |
| Start | 141574035:141574035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1815T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389054 |
| Start | 141528496:141528496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3105C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389054 |
| Start | 141580758:141580758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745385668 |
| CDS Mutation | c.810G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |