Primary Site >> Stomach Cancer
Gene >> OPTN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263036 |
| Start | 13127803:13127803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1301A>C |
| AA Mutation | p.Glu434Ala(p.E434A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263036 |
| Start | 13136765:13136765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774245711 |
| CDS Mutation | c.1633C>T |
| AA Mutation | p.Arg545Trp(p.R545W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263036 |
| Start | 13112606:13112606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.523G>C |
| AA Mutation | p.Glu175Gln(p.E175Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263036 |
| Start | 13112615:13112615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.532T>G |
| AA Mutation | p.Phe178Val(p.F178V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263036 |
| Start | 13132190:13132190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182957382 |
| CDS Mutation | c.1525G>A |
| AA Mutation | p.Gly509Arg(p.G509R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263036 |
| Start | 13124057:13124057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.945G>T |
| AA Mutation | p.Glu315Asp(p.E315D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263036 |
| Start | 13127777:13127777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1275A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263036 |
| Start | 13124075:13124075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150381274 |
| CDS Mutation | c.963C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263036 |
| Start | 13112533:13112533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778511187 |
| CDS Mutation | c.450A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263036 |
| Start | 13132160:13132160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1495C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263036 |
| Start | 13126010:13126010(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1216delA |
| AA Mutation | p.Thr406GlnfsTer5(p.T406Qfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263036 |
| Start | 13109192:13109192(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs766608795 |
| CDS Mutation | c.76delC |
| AA Mutation | p.His26ThrfsTer19(p.H26Tfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000263036 |
| Start | 13109191:13109192(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs753966040 |
| CDS Mutation | c.76dupC |
| AA Mutation | p.His26ProfsTer37(p.H26Pfs*37) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |