Primary Site >> Stomach Cancer
Gene >> DNMT3L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000628202 |
| Start | 44259533:44259533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757132660 |
| CDS Mutation | c.248C>T |
| AA Mutation | p.Ala83Val(p.A83V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000628202 |
| Start | 44259510:44259510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770222665 |
| CDS Mutation | c.271G>A |
| AA Mutation | p.Gly91Arg(p.G91R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000628202 |
| Start | 44259504:44259504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.277C>A |
| AA Mutation | p.Gln93Lys(p.Q93K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000628202 |
| Start | 44259531:44259531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.250C>A |
| AA Mutation | p.Leu84Ile(p.L84I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000628202 |
| Start | 44261252:44261252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8C>T |
| AA Mutation | p.Ala3Val(p.A3V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000628202 |
| Start | 44260807:44260807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368058982 |
| CDS Mutation | c.139C>T |
| AA Mutation | p.Arg47Ter(p.R47*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000628202 |
| Start | 44256156:44256156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.517-2A>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |