Primary Site >> Stomach Cancer
Gene >> MTRR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264668 |
| Start | 7873461:7873461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.299T>G |
| AA Mutation | p.Val100Gly(p.V100G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264668 |
| Start | 7875294:7875294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.401G>A |
| AA Mutation | p.Gly134Glu(p.G134E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264668 |
| Start | 7897084:7897084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755408035 |
| CDS Mutation | c.1870C>A |
| AA Mutation | p.Leu624Ile(p.L624I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264668 |
| Start | 7892810:7892810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146475928 |
| CDS Mutation | c.1535G>A |
| AA Mutation | p.Arg512Gln(p.R512Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264668 |
| Start | 7896890:7896890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1784A>G |
| AA Mutation | p.Asp595Gly(p.D595G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264668 |
| Start | 7875371:7875371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770923981 |
| CDS Mutation | c.478G>A |
| AA Mutation | p.Val160Ile(p.V160I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264668 |
| Start | 7878038:7878038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114253881 |
| CDS Mutation | c.577G>T |
| AA Mutation | p.Ala193Ser(p.A193S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264668 |
| Start | 7873452:7873452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777202031 |
| CDS Mutation | c.290G>A |
| AA Mutation | p.Arg97His(p.R97H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264668 |
| Start | 7883203:7883203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.910C>T |
| AA Mutation | p.Pro304Ser(p.P304S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264668 |
| Start | 7889131:7889131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1264A>G |
| AA Mutation | p.Ser422Gly(p.S422G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264668 |
| Start | 7873387:7873387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138612190 |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264668 |
| Start | 7869151:7869151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.18G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264668 |
| Start | 7878278:7878278(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs752858024 |
| CDS Mutation | c.821delC |
| AA Mutation | p.Pro274GlnfsTer21(p.P274Qfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |