Primary Site >> Stomach Cancer
Gene >> SEMA7A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261918 |
| Start | 74410632:74410632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1993G>T |
| AA Mutation | p.Val665Phe(p.V665F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261918 |
| Start | 74414678:74414678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771532027 |
| CDS Mutation | c.1163C>T |
| AA Mutation | p.Ala388Val(p.A388V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261918 |
| Start | 74411664:74411664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1469T>C |
| AA Mutation | p.Leu490Pro(p.L490P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261918 |
| Start | 74417371:74417371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767503529 |
| CDS Mutation | c.625G>A |
| AA Mutation | p.Glu209Lys(p.E209K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261918 |
| Start | 74411328:74411328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1606G>A |
| AA Mutation | p.Glu536Lys(p.E536K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261918 |
| Start | 74415969:74415969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.818A>G |
| AA Mutation | p.Glu273Gly(p.E273G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261918 |
| Start | 74410893:74410893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763712355 |
| CDS Mutation | c.1732C>T |
| AA Mutation | p.Arg578Cys(p.R578C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261918 |
| Start | 74410943:74410943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1682G>A |
| AA Mutation | p.Arg561His(p.R561H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261918 |
| Start | 74410825:74410825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781291005 |
| CDS Mutation | c.1800C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000261918 |
| Start | 74416574:74416574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.801+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |