Primary Site >> Stomach Cancer
Gene >> PPAT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264220 |
| Start | 56401453:56401453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.763A>G |
| AA Mutation | p.Ile255Val(p.I255V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264220 |
| Start | 56406514:56406514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.383C>G |
| AA Mutation | p.Ala128Gly(p.A128G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264220 |
| Start | 56401425:56401425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.791A>G |
| AA Mutation | p.Gln264Arg(p.Q264R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264220 |
| Start | 56406671:56406671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.226G>A |
| AA Mutation | p.Glu76Lys(p.E76K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264220 |
| Start | 56395488:56395488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1418T>C |
| AA Mutation | p.Ile473Thr(p.I473T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264220 |
| Start | 56396635:56396635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770073845 |
| CDS Mutation | c.1341C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264220 |
| Start | 56403083:56403083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.618A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264220 |
| Start | 56406531:56406531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749766197 |
| CDS Mutation | c.366T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |