Primary Site >> Stomach Cancer
Gene >> PLEKHG5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400915 |
| Start | 6473111:6473111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1027A>G |
| AA Mutation | p.Arg343Gly(p.R343G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400915 |
| Start | 6474517:6474517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.541T>A |
| AA Mutation | p.Ser181Thr(p.S181T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400915 |
| Start | 6477616:6477616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.124C>G |
| AA Mutation | p.Pro42Ala(p.P42A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400915 |
| Start | 6471069:6471069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1481A>G |
| AA Mutation | p.Tyr494Cys(p.Y494C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400915 |
| Start | 6470330:6470330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1874A>G |
| AA Mutation | p.Asp625Gly(p.D625G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400915 |
| Start | 6469389:6469389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2163G>T |
| AA Mutation | p.Gln721His(p.Q721H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000400915 |
| Start | 6470300:6470300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757727499 |
| CDS Mutation | c.1904C>T |
| AA Mutation | p.Pro635Leu(p.P635L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400915 |
| Start | 6473096:6473096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1042C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400915 |
| Start | 6496517:6496517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533070676 |
| CDS Mutation | c.57C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400915 |
| Start | 6470512:6470512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1842G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400915 |
| Start | 6474090:6474090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748476669 |
| CDS Mutation | c.682C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000400915 |
| Start | 6470518:6470518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1836C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |