Primary Site >> Stomach Cancer
Gene >> SPARC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231061 |
| Start | 151671678:151671678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.225C>A |
| AA Mutation | p.His75Gln(p.H75Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231061 |
| Start | 151667520:151667520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.532C>A |
| AA Mutation | p.Leu178Met(p.L178M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231061 |
| Start | 151671623:151671623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142207246 |
| CDS Mutation | c.280G>A |
| AA Mutation | p.Val94Met(p.V94M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231061 |
| Start | 151664183:151664183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.787G>A |
| AA Mutation | p.Glu263Lys(p.E263K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231061 |
| Start | 151664126:151664126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532217814 |
| CDS Mutation | c.844G>A |
| AA Mutation | p.Ala282Thr(p.A282T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231061 |
| Start | 151664110:151664110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.860C>T |
| AA Mutation | p.Ala287Val(p.A287V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000231061 |
| Start | 151666390:151666390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755476160 |
| CDS Mutation | c.705C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000231061 |
| Start | 151664220:151664220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.750C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000231061 |
| Start | 151667569:151667569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376445735 |
| CDS Mutation | c.483C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |