Primary Site >> Stomach Cancer
Gene >> CORO7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251166 |
| Start | 4407511:4407511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.477G>T |
| AA Mutation | p.Gln159His(p.Q159H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251166 |
| Start | 4359527:4359527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2203C>A |
| AA Mutation | p.Leu735Met(p.L735M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251166 |
| Start | 4365044:4365044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.857A>G |
| AA Mutation | p.Tyr286Cys(p.Y286C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251166 |
| Start | 4359581:4359581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2149C>A |
| AA Mutation | p.Leu717Met(p.L717M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251166 |
| Start | 4359545:4359545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200550834 |
| CDS Mutation | c.2185G>A |
| AA Mutation | p.Val729Met(p.V729M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251166 |
| Start | 4358007:4358007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2554C>T |
| AA Mutation | p.Pro852Ser(p.P852S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251166 |
| Start | 4413374:4413374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143239749 |
| CDS Mutation | c.91G>A |
| AA Mutation | p.Ala31Thr(p.A31T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251166 |
| Start | 4361441:4361441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145925246 |
| CDS Mutation | c.1607C>T |
| AA Mutation | p.Thr536Met(p.T536M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251166 |
| Start | 4362677:4362677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1337C>A |
| AA Mutation | p.Pro446His(p.P446H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251166 |
| Start | 4361079:4361079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201451820 |
| CDS Mutation | c.1781C>T |
| AA Mutation | p.Thr594Met(p.T594M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251166 |
| Start | 4360337:4360337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199645423 |
| CDS Mutation | c.2049C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251166 |
| Start | 4364844:4364844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139939383 |
| CDS Mutation | c.975C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000251166 |
| Start | 4407672:4407672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745958172 |
| CDS Mutation | c.316C>T |
| AA Mutation | p.Arg106Ter(p.R106*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |