Primary Site >> Stomach Cancer
Gene >> PRB2
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000389362 |
| Start | 11393977:11393977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.101G>A |
| AA Mutation | p.Gly34Glu(p.G34E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389362 |
| Start | 11392982:11392982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1096C>T |
| AA Mutation | p.Pro366Ser(p.P366S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389362 |
| Start | 11392913:11392913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1165C>A |
| AA Mutation | p.Gln389Lys(p.Q389K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389362 |
| Start | 11393971:11393971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758708990 |
| CDS Mutation | c.107C>T |
| AA Mutation | p.Pro36Leu(p.P36L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389362 |
| Start | 11393811:11393811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758143951 |
| CDS Mutation | c.267T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389362 |
| Start | 11393830:11393830(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.248delC |
| AA Mutation | p.Pro83HisfsTer348(p.P83Hfs*348) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |