Primary Site >> Stomach Cancer
Gene >> PRMT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454376 |
| Start | 49688228:49688228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1099G>A |
| AA Mutation | p.Asp367Asn(p.D367N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454376 |
| Start | 49688189:49688189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1060G>C |
| AA Mutation | p.Asp354His(p.D354H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454376 |
| Start | 49684997:49684997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.719T>C |
| AA Mutation | p.Val240Ala(p.V240A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454376 |
| Start | 49686162:49686162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765879950 |
| CDS Mutation | c.829C>T |
| AA Mutation | p.Arg277Trp(p.R277W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454376 |
| Start | 49679912:49679912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.77C>T |
| AA Mutation | p.Pro26Leu(p.P26L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454376 |
| Start | 49688212:49688212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769054141 |
| CDS Mutation | c.1083G>T |
| AA Mutation | p.Glu361Asp(p.E361D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000454376 |
| Start | 49686702:49686702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1008C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000454376 |
| Start | 49686639:49686639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs181508065 |
| CDS Mutation | c.945G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000454376 |
| Start | 49681924:49681924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746258178 |
| CDS Mutation | c.207C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000454376 |
| Start | 49686230:49686230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188991153 |
| CDS Mutation | c.897C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |