Primary Site >> Stomach Cancer
Gene >> IL6ST
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336909 |
| Start | 55951487:55951487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1817T>C |
| AA Mutation | p.Phe606Ser(p.F606S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336909 |
| Start | 55941638:55941638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774424754 |
| CDS Mutation | c.2201T>C |
| AA Mutation | p.Met734Thr(p.M734T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336909 |
| Start | 55941726:55941726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2113C>T |
| AA Mutation | p.Pro705Ser(p.P705S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336909 |
| Start | 55964194:55964194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.610C>A |
| AA Mutation | p.Leu204Ile(p.L204I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336909 |
| Start | 55964187:55964187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.617A>C |
| AA Mutation | p.Lys206Thr(p.K206T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336909 |
| Start | 55952029:55952029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539735402 |
| CDS Mutation | c.1599C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336909 |
| Start | 55941151:55941151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766571216 |
| CDS Mutation | c.2688G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336909 |
| Start | 55941379:55941379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2460T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000336909 |
| Start | 55952041:55952041(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776023104 |
| CDS Mutation | c.1587delA |
| AA Mutation | p.Val530Ter(p.V530*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |