Primary Site >> Stomach Cancer
Gene >> TMEM245
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374586 |
| Start | 109036299:109036299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2306C>T |
| AA Mutation | p.Thr769Ile(p.T769I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374586 |
| Start | 109057299:109057299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1746C>G |
| AA Mutation | p.His582Gln(p.H582Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374586 |
| Start | 109108537:109108537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.613G>T |
| AA Mutation | p.Val205Phe(p.V205F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374586 |
| Start | 109091041:109091041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751906384 |
| CDS Mutation | c.1031C>T |
| AA Mutation | p.Thr344Met(p.T344M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374586 |
| Start | 109033357:109033357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766218648 |
| CDS Mutation | c.2544G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374586 |
| Start | 109064522:109064522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138324371 |
| CDS Mutation | c.1578G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000374586 |
| Start | 109036351:109036352(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2245_2253dupGCAGTGCCA |
| AA Mutation | p.Ala749_Pro751dup(p.A749_P751dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |