Primary Site >> Stomach Cancer
Gene >> SATB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260926 |
| Start | 199272337:199272337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2076G>T |
| AA Mutation | p.Glu692Asp(p.E692D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260926 |
| Start | 199272344:199272344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2069A>T |
| AA Mutation | p.Lys690Met(p.K690M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260926 |
| Start | 199349012:199349012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142825652 |
| CDS Mutation | c.862G>A |
| AA Mutation | p.Ala288Thr(p.A288T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260926 |
| Start | 199272534:199272534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1879G>T |
| AA Mutation | p.Gly627Trp(p.G627W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260926 |
| Start | 199349086:199349086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.788C>A |
| AA Mutation | p.Ser263Tyr(p.S263Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260926 |
| Start | 199348706:199348706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1168A>G |
| AA Mutation | p.Thr390Ala(p.T390A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260926 |
| Start | 199308800:199308800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1700G>A |
| AA Mutation | p.Arg567His(p.R567H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260926 |
| Start | 199272365:199272365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2048C>T |
| AA Mutation | p.Ala683Val(p.A683V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260926 |
| Start | 199380377:199380377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.584G>A |
| AA Mutation | p.Cys195Tyr(p.C195Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260926 |
| Start | 199381747:199381747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202223477 |
| CDS Mutation | c.420C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260926 |
| Start | 199348908:199348908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139350909 |
| CDS Mutation | c.966C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260926 |
| Start | 199433384:199433384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776492115 |
| CDS Mutation | c.300G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260926 |
| Start | 199433441:199433441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372121244 |
| CDS Mutation | c.243C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260926 |
| Start | 199433351:199433351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140116634 |
| CDS Mutation | c.333G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260926 |
| Start | 199433405:199433405(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.279delT |
| AA Mutation | p.Phe93LeufsTer25(p.F93Lfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260926 |
| Start | 199272257:199272257(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2156delA |
| AA Mutation | p.Asn719MetfsTer21(p.N719Mfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000260926 |
| Start | 199349084:199349085(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.789_790insAAGTTGTGGACTAAG |
| AA Mutation | p.Ser263_Leu264insLysLeuTrpThrLys(p.S263_L264insKLWTK) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |