Primary Site >> Stomach Cancer
Gene >> PRLHR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239032 |
| Start | 118594941:118594941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.304C>A |
| AA Mutation | p.Leu102Met(p.L102M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239032 |
| Start | 118594754:118594754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.491T>C |
| AA Mutation | p.Val164Ala(p.V164A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239032 |
| Start | 118595121:118595121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.124G>A |
| AA Mutation | p.Ala42Thr(p.A42T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239032 |
| Start | 118594326:118594326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.919G>A |
| AA Mutation | p.Ala307Thr(p.A307T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239032 |
| Start | 118594932:118594932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.313T>C |
| AA Mutation | p.Ser105Pro(p.S105P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239032 |
| Start | 118595132:118595132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.113C>T |
| AA Mutation | p.Ser38Leu(p.S38L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239032 |
| Start | 118594869:118594869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.376G>A |
| AA Mutation | p.Gly126Ser(p.G126S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239032 |
| Start | 118594380:118594380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.865G>A |
| AA Mutation | p.Val289Ile(p.V289I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239032 |
| Start | 118594980:118594980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.265C>T |
| AA Mutation | p.Arg89Cys(p.R89C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000239032 |
| Start | 118595136:118595136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763541855 |
| CDS Mutation | c.109G>A |
| AA Mutation | p.Gly37Arg(p.G37R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |