Primary Site >> Stomach Cancer
Gene >> CBLB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264122 |
| Start | 105659193:105659193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371406651 |
| CDS Mutation | c.2726G>A |
| AA Mutation | p.Arg909Gln(p.R909Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264122 |
| Start | 105681784:105681784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2236A>G |
| AA Mutation | p.Thr746Ala(p.T746A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264122 |
| Start | 105751495:105751495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.690T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264122 |
| Start | 105659195:105659195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2724A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264122 |
| Start | 105659138:105659138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374734212 |
| CDS Mutation | c.2781G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264122 |
| Start | 105659174:105659174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2745A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264122 |
| Start | 105681513:105681513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780851468 |
| CDS Mutation | c.2394G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |