Primary Site >> Esophagus Cancer
Gene >> ADAMTS9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000498707 |
| Start | 64541190:64541190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150104451 |
| CDS Mutation | c.5426G>A |
| AA Mutation | p.Arg1809Gln(p.R1809Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000498707 |
| Start | 64596966:64596966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4043C>A |
| AA Mutation | p.Ser1348Tyr(p.S1348Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000498707 |
| Start | 64651139:64651139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1341C>A |
| AA Mutation | p.Asn447Lys(p.N447K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000498707 |
| Start | 64613502:64613502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3197T>G |
| AA Mutation | p.Val1066Gly(p.V1066G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000498707 |
| Start | 64616122:64616122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2862T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000498707 |
| Start | 64658652:64658652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373657194 |
| CDS Mutation | c.819G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000498707 |
| Start | 64686940:64686940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.144C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |