Primary Site >> Stomach Cancer
Gene >> SPAG9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262013 |
| Start | 50974917:50974917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142387747 |
| CDS Mutation | c.3554G>A |
| AA Mutation | p.Arg1185His(p.R1185H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262013 |
| Start | 50979895:50979895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3260G>T |
| AA Mutation | p.Arg1087Met(p.R1087M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262013 |
| Start | 51021338:51021338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.811G>A |
| AA Mutation | p.Gly271Arg(p.G271R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262013 |
| Start | 50996672:50996672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1861C>T |
| AA Mutation | p.Arg621Cys(p.R621C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262013 |
| Start | 50977159:50977159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3472T>G |
| AA Mutation | p.Leu1158Val(p.L1158V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262013 |
| Start | 50970737:50970737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3820G>A |
| AA Mutation | p.Gly1274Arg(p.G1274R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262013 |
| Start | 50989794:50989794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768131495 |
| CDS Mutation | c.2696C>T |
| AA Mutation | p.Ala899Val(p.A899V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262013 |
| Start | 50996644:50996644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758187012 |
| CDS Mutation | c.1889G>A |
| AA Mutation | p.Arg630His(p.R630H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262013 |
| Start | 51041643:51041643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139684309 |
| CDS Mutation | c.599G>A |
| AA Mutation | p.Arg200His(p.R200H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262013 |
| Start | 51021255:51021255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763174207 |
| CDS Mutation | c.894C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262013 |
| Start | 50990532:50990532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2535T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262013 |
| Start | 50970852:50970852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3705A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262013 |
| Start | 50998518:50998518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374965775 |
| CDS Mutation | c.1764C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262013 |
| Start | 50999680:50999680(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776201899 |
| CDS Mutation | c.1645delA |
| AA Mutation | p.Arg549GlyfsTer28(p.R549Gfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |