Primary Site >> Stomach Cancer
Gene >> MAP1S
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324096 |
| Start | 17725925:17725925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752078894 |
| CDS Mutation | c.541G>A |
| AA Mutation | p.Ala181Thr(p.A181T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324096 |
| Start | 17726433:17726433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1049G>A |
| AA Mutation | p.Arg350His(p.R350H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324096 |
| Start | 17734321:17734321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371306436 |
| CDS Mutation | c.3073G>A |
| AA Mutation | p.Ala1025Thr(p.A1025T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324096 |
| Start | 17725980:17725980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.596C>T |
| AA Mutation | p.Ala199Val(p.A199V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324096 |
| Start | 17727801:17727801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2417C>T |
| AA Mutation | p.Ala806Val(p.A806V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324096 |
| Start | 17727578:17727578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2194C>T |
| AA Mutation | p.Pro732Ser(p.P732S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324096 |
| Start | 17726168:17726168(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.784A>G |
| AA Mutation | p.Thr262Ala(p.T262A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324096 |
| Start | 17734299:17734299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3051G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324096 |
| Start | 17733386:17733386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147584152 |
| CDS Mutation | c.2982C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324096 |
| Start | 17727634:17727634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758396147 |
| CDS Mutation | c.2250G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000324096 |
| Start | 17725852:17725852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747118489 |
| CDS Mutation | c.468G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |