Primary Site >> Stomach Cancer
Gene >> SATB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18394754:18394754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.914C>A |
| AA Mutation | p.Pro305His(p.P305H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18352128:18352128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1643A>G |
| AA Mutation | p.Asn548Ser(p.N548S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18349331:18349331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776281718 |
| CDS Mutation | c.2131G>A |
| AA Mutation | p.Gly711Ser(p.G711S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18386479:18386479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1339G>A |
| AA Mutation | p.Glu447Lys(p.E447K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18352084:18352084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1687C>T |
| AA Mutation | p.Arg563Cys(p.R563C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18415169:18415169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.581A>C |
| AA Mutation | p.Lys194Thr(p.K194T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18416059:18416059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.463G>C |
| AA Mutation | p.Asp155His(p.D155H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18349448:18349448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2014G>A |
| AA Mutation | p.Glu672Lys(p.E672K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18386409:18386409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1409G>A |
| AA Mutation | p.Arg470His(p.R470H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18386589:18386589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1229G>A |
| AA Mutation | p.Arg410Gln(p.R410Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18394601:18394601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1067C>A |
| AA Mutation | p.Ser356Tyr(p.S356Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338745 |
| Start | 18349573:18349573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777236078 |
| CDS Mutation | c.1889C>T |
| AA Mutation | p.Thr630Met(p.T630M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338745 |
| Start | 18349467:18349467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763259243 |
| CDS Mutation | c.1995C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338745 |
| Start | 18394501:18394501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1167C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338745 |
| Start | 18394492:18394492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1176A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338745 |
| Start | 18416093:18416093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.429T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338745 |
| Start | 18352028:18352028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147456964 |
| CDS Mutation | c.1743G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338745 |
| Start | 18349572:18349572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769372550 |
| CDS Mutation | c.1890G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338745 |
| Start | 18352007:18352007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1764A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338745 |
| Start | 18420905:18420905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.63T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338745 |
| Start | 18349585:18349585(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1877delC |
| AA Mutation | p.Pro626HisfsTer81(p.P626Hfs*81) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338745 |
| Start | 18349238:18349238(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2224delT |
| AA Mutation | p.Ser742GlnfsTer2(p.S742Qfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338745 |
| Start | 18415119:18415119(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.631delC |
| AA Mutation | p.Leu211PhefsTer5(p.L211Ffs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000338745 |
| Start | 18349538:18349538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752755275 |
| CDS Mutation | c.1924C>T |
| AA Mutation | p.Arg642Ter(p.R642*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |