Primary Site >> Stomach Cancer
Gene >> ESR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206249 |
| Start | 152098959:152098959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138891155 |
| CDS Mutation | c.1781C>T |
| AA Mutation | p.Thr594Met(p.T594M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206249 |
| Start | 152011686:152011686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1127T>C |
| AA Mutation | p.Val376Ala(p.V376A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206249 |
| Start | 151807949:151807949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761420991 |
| CDS Mutation | c.37G>A |
| AA Mutation | p.Ala13Thr(p.A13T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206249 |
| Start | 151808114:151808114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771540162 |
| CDS Mutation | c.202G>A |
| AA Mutation | p.Ala68Thr(p.A68T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206249 |
| Start | 151944344:151944344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766779326 |
| CDS Mutation | c.932C>T |
| AA Mutation | p.Thr311Met(p.T311M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206249 |
| Start | 152098775:152098775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778116774 |
| CDS Mutation | c.1597G>A |
| AA Mutation | p.Val533Met(p.V533M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206249 |
| Start | 151944472:151944472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1060C>A |
| AA Mutation | p.Leu354Met(p.L354M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206249 |
| Start | 151880730:151880730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.719G>A |
| AA Mutation | p.Cys240Tyr(p.C240Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000206249 |
| Start | 151842598:151842598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.454C>A |
| AA Mutation | p.Pro152Thr(p.P152T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000206249 |
| Start | 152098813:152098813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201562714 |
| CDS Mutation | c.1635C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000206249 |
| Start | 152094480:152094480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767627349 |
| CDS Mutation | c.1465C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000206249 |
| Start | 151880749:151880749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.738C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000206249 |
| Start | 151808203:151808203(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.296delC |
| AA Mutation | p.Pro99HisfsTer10(p.P99Hfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000206249 |
| Start | 152094444:152094444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762742833 |
| CDS Mutation | c.1429C>T |
| AA Mutation | p.Arg477Ter(p.R477*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |