Primary Site >> Stomach Cancer
Gene >> PNMT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269582 |
| Start | 39670082:39670082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.542C>T |
| AA Mutation | p.Ala181Val(p.A181V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269582 |
| Start | 39670148:39670148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111272760 |
| CDS Mutation | c.608C>T |
| AA Mutation | p.Thr203Met(p.T203M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269582 |
| Start | 39670318:39670318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.778G>A |
| AA Mutation | p.Ala260Thr(p.A260T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269582 |
| Start | 39669760:39669760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34530498 |
| CDS Mutation | c.334C>T |
| AA Mutation | p.Arg112Cys(p.R112C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269582 |
| Start | 39669986:39669986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.446C>T |
| AA Mutation | p.Ala149Val(p.A149V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269582 |
| Start | 39670274:39670274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748756615 |
| CDS Mutation | c.734G>A |
| AA Mutation | p.Arg245His(p.R245H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269582 |
| Start | 39669973:39669973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768713506 |
| CDS Mutation | c.433C>T |
| AA Mutation | p.Arg145Cys(p.R145C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269582 |
| Start | 39669974:39669974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150323544 |
| CDS Mutation | c.434G>A |
| AA Mutation | p.Arg145His(p.R145H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000269582 |
| Start | 39670068:39670068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749507897 |
| CDS Mutation | c.528C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |