Primary Site >> Stomach Cancer
Gene >> MYO1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300119 |
| Start | 57041251:57041251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1202A>T |
| AA Mutation | p.Asn401Ile(p.N401I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300119 |
| Start | 57048036:57048036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.183C>A |
| AA Mutation | p.Phe61Leu(p.F61L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300119 |
| Start | 57038497:57038497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372055709 |
| CDS Mutation | c.1675C>T |
| AA Mutation | p.Arg559Cys(p.R559C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300119 |
| Start | 57031102:57031102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769645609 |
| CDS Mutation | c.2422G>A |
| AA Mutation | p.Ala808Thr(p.A808T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300119 |
| Start | 57038632:57038632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1540T>C |
| AA Mutation | p.Tyr514His(p.Y514H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300119 |
| Start | 57038517:57038517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1655C>A |
| AA Mutation | p.Pro552His(p.P552H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300119 |
| Start | 57029819:57029819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2645T>C |
| AA Mutation | p.Leu882Pro(p.L882P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000300119 |
| Start | 57046884:57046884(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.520delC |
| AA Mutation | p.Leu174SerfsTer15(p.L174Sfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000300119 |
| Start | 57028789:57028789(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs770612489 |
| CDS Mutation | c.3098delA |
| AA Mutation | p.Lys1033ArgfsTer8(p.K1033Rfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |