Primary Site >> Stomach Cancer
Gene >> GFM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000486715 |
| Start | 158652137:158652137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150903461 |
| CDS Mutation | c.731C>T |
| AA Mutation | p.Ala244Val(p.A244V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000486715 |
| Start | 158646196:158646196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.266T>C |
| AA Mutation | p.Met89Thr(p.M89T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000486715 |
| Start | 158646832:158646832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.457T>C |
| AA Mutation | p.Cys153Arg(p.C153R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000486715 |
| Start | 158646866:158646866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200727254 |
| CDS Mutation | c.491G>A |
| AA Mutation | p.Arg164His(p.R164H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000486715 |
| Start | 158652242:158652242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.836T>C |
| AA Mutation | p.Leu279Ser(p.L279S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000486715 |
| Start | 158652162:158652162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.756G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000486715 |
| Start | 158645664:158645664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.117G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000486715 |
| Start | 158684541:158684541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141903395 |
| CDS Mutation | c.1782C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000486715 |
| Start | 158646233:158646234(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.304_305delAT |
| AA Mutation | p.Ile102SerfsTer15(p.I102Sfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000486715 |
| Start | 158645677:158645678(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.136dupA |
| AA Mutation | p.Ile46AsnfsTer11(p.I46Nfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |