Primary Site >> Stomach Cancer
Gene >> MTNR1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257068 |
| Start | 92981828:92981828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774779129 |
| CDS Mutation | c.605C>T |
| AA Mutation | p.Ala202Val(p.A202V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257068 |
| Start | 92969879:92969879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369464202 |
| CDS Mutation | c.154G>A |
| AA Mutation | p.Ala52Thr(p.A52T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257068 |
| Start | 92981768:92981768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.545A>C |
| AA Mutation | p.Glu182Ala(p.E182A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257068 |
| Start | 92969918:92969918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758044308 |
| CDS Mutation | c.193G>A |
| AA Mutation | p.Val65Met(p.V65M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257068 |
| Start | 92982263:92982263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1040G>A |
| AA Mutation | p.Ser347Asn(p.S347N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257068 |
| Start | 92969887:92969887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774326577 |
| CDS Mutation | c.162C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |