Primary Site >> Stomach Cancer
Gene >> PROCR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216968 |
| Start | 35176239:35176239(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.394G>A |
| AA Mutation | p.Glu132Lys(p.E132K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216968 |
| Start | 35176171:35176171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.326C>A |
| AA Mutation | p.Pro109His(p.P109H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216968 |
| Start | 35176279:35176279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144485700 |
| CDS Mutation | c.434C>T |
| AA Mutation | p.Pro145Leu(p.P145L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216968 |
| Start | 35176246:35176246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.401C>A |
| AA Mutation | p.Ala134Asp(p.A134D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216968 |
| Start | 35176262:35176262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.417C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216968 |
| Start | 35176433:35176433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779402481 |
| CDS Mutation | c.588G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216968 |
| Start | 35176726:35176726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs558494965 |
| CDS Mutation | c.630G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |