Primary Site >> Stomach Cancer
Gene >> SLCO2A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310926 |
| Start | 134029799:134029799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4G>A |
| AA Mutation | p.Gly2Arg(p.G2R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310926 |
| Start | 133953684:133953684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.703G>A |
| AA Mutation | p.Asp235Asn(p.D235N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310926 |
| Start | 133934810:133934810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1835G>A |
| AA Mutation | p.Gly612Asp(p.G612D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310926 |
| Start | 133973702:133973702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.358T>C |
| AA Mutation | p.Phe120Leu(p.F120L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310926 |
| Start | 133942649:133942649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1581G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310926 |
| Start | 133954976:133954976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.615C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310926 |
| Start | 133942751:133942751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1479C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310926 |
| Start | 133954979:133954979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763713775 |
| CDS Mutation | c.612G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310926 |
| Start | 133945209:133945209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373457618 |
| CDS Mutation | c.1347G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310926 |
| Start | 133979550:133979550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.165C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310926 |
| Start | 133945247:133945247(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1309delA |
| AA Mutation | p.Ile437TyrfsTer43(p.I437Yfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310926 |
| Start | 133951239:133951239(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs765906270 |
| CDS Mutation | c.830delT |
| AA Mutation | p.Phe277SerfsTer8(p.F277Sfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |