Primary Site >> Stomach Cancer
Gene >> PRLR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618457 |
| Start | 35086299:35086299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.112T>C |
| AA Mutation | p.Ser38Pro(p.S38P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618457 |
| Start | 35065735:35065735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1223C>T |
| AA Mutation | p.Ala408Val(p.A408V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618457 |
| Start | 35072595:35072595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762980564 |
| CDS Mutation | c.523G>A |
| AA Mutation | p.Glu175Lys(p.E175K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618457 |
| Start | 35086226:35086226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.185T>C |
| AA Mutation | p.Leu62Pro(p.L62P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618457 |
| Start | 35068863:35068863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.701A>G |
| AA Mutation | p.Asp234Gly(p.D234G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000618457 |
| Start | 35066030:35066030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.928T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000618457 |
| Start | 35084483:35084483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745809333 |
| CDS Mutation | c.360C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |