Primary Site >> Stomach Cancer
Gene >> SOCS6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397942 |
| Start | 70325822:70325822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1154A>G |
| AA Mutation | p.Tyr385Cys(p.Y385C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397942 |
| Start | 70325521:70325521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766296683 |
| CDS Mutation | c.853G>A |
| AA Mutation | p.Val285Met(p.V285M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397942 |
| Start | 70325882:70325882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1214C>A |
| AA Mutation | p.Ser405Tyr(p.S405Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397942 |
| Start | 70326095:70326095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749608539 |
| CDS Mutation | c.1427G>A |
| AA Mutation | p.Arg476Gln(p.R476Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397942 |
| Start | 70325173:70325173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766434830 |
| CDS Mutation | c.505A>G |
| AA Mutation | p.Asn169Asp(p.N169D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397942 |
| Start | 70324857:70324857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs41328646 |
| CDS Mutation | c.189C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397942 |
| Start | 70325886:70325886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1218T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397942 |
| Start | 70325520:70325520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200886437 |
| CDS Mutation | c.852C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397942 |
| Start | 70324859:70324860(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.197dupA |
| AA Mutation | p.Asn66LysfsTer49(p.N66Kfs*49) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |