Primary Site >> Stomach Cancer
Gene >> HELLS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348459 |
| Start | 94574164:94574164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.682G>A |
| AA Mutation | p.Val228Ile(p.V228I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348459 |
| Start | 94576728:94576728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555694666 |
| CDS Mutation | c.955C>T |
| AA Mutation | p.Arg319Trp(p.R319W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348459 |
| Start | 94554165:94554165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.193T>C |
| AA Mutation | p.Tyr65His(p.Y65H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348459 |
| Start | 94594726:94594726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2120G>A |
| AA Mutation | p.Arg707Lys(p.R707K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000348459 |
| Start | 94554126:94554126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.154G>A |
| AA Mutation | p.Ala52Thr(p.A52T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000348459 |
| Start | 94592495:94592495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1952A>G |
| AA Mutation | p.Tyr651Cys(p.Y651C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000348459 |
| Start | 94546377:94546377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.32G>A |
| AA Mutation | p.Gly11Asp(p.G11D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348459 |
| Start | 94593600:94593600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2073T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348459 |
| Start | 94590770:94590770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1761A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000348459 |
| Start | 94588243:94588243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1341C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000348459 |
| Start | 94592294:94592294(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs745837238 |
| CDS Mutation | c.1840delA |
| AA Mutation | p.Arg614GlufsTer11(p.R614Efs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |