Primary Site >> Stomach Cancer
Gene >> SLCO3A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 92162902:92162902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1900A>G |
| AA Mutation | p.Lys634Glu(p.K634E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 91916422:91916422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745409648 |
| CDS Mutation | c.610G>A |
| AA Mutation | p.Asp204Asn(p.D204N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 92126150:92126150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745557536 |
| CDS Mutation | c.1264C>T |
| AA Mutation | p.Arg422Trp(p.R422W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 92162816:92162816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1814G>A |
| AA Mutation | p.Ser605Asn(p.S605N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 91854063:91854063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.155C>T |
| AA Mutation | p.Ala52Val(p.A52V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 92162870:92162870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1868G>A |
| AA Mutation | p.Arg623Gln(p.R623Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 92104401:92104401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.868C>T |
| AA Mutation | p.Pro290Ser(p.P290S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 91916191:91916191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.379G>A |
| AA Mutation | p.Glu127Lys(p.E127K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 92120591:92120591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1136A>G |
| AA Mutation | p.Gln379Arg(p.Q379R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 92162947:92162947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1945A>T |
| AA Mutation | p.Arg649Trp(p.R649W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318445 |
| Start | 92162896:92162896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369481876 |
| CDS Mutation | c.1894G>A |
| AA Mutation | p.Ala632Thr(p.A632T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318445 |
| Start | 91916145:91916145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760273166 |
| CDS Mutation | c.333C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318445 |
| Start | 92126191:92126191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140581310 |
| CDS Mutation | c.1305C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318445 |
| Start | 91916427:91916427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318445 |
| Start | 92126071:92126071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762980183 |
| CDS Mutation | c.1185G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |