Primary Site >> Stomach Cancer
Gene >> SALL4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790354:51790354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761020459 |
| CDS Mutation | c.2129C>T |
| AA Mutation | p.Thr710Met(p.T710M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791428:51791428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754206289 |
| CDS Mutation | c.1055C>T |
| AA Mutation | p.Ala352Val(p.A352V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791252:51791252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1231G>A |
| AA Mutation | p.Val411Met(p.V411M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790189:51790189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2294C>T |
| AA Mutation | p.Ser765Leu(p.S765L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791110:51791110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1373C>T |
| AA Mutation | p.Ala458Val(p.A458V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791396:51791396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759061679 |
| CDS Mutation | c.1087C>T |
| AA Mutation | p.Pro363Ser(p.P363S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51792299:51792299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767807086 |
| CDS Mutation | c.184A>G |
| AA Mutation | p.Thr62Ala(p.T62A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51792073:51792073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.410G>A |
| AA Mutation | p.Gly137Asp(p.G137D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790255:51790255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2228T>C |
| AA Mutation | p.Leu743Pro(p.L743P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791341:51791341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1142A>C |
| AA Mutation | p.Lys381Thr(p.K381T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791033:51791033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1450G>T |
| AA Mutation | p.Gly484Trp(p.G484W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791534:51791534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.949C>T |
| AA Mutation | p.Pro317Ser(p.P317S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790108:51790108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779778006 |
| CDS Mutation | c.2375A>G |
| AA Mutation | p.Asn792Ser(p.N792S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51784483:51784483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778170676 |
| CDS Mutation | c.2944G>A |
| AA Mutation | p.Val982Met(p.V982M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790087:51790087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2396A>G |
| AA Mutation | p.Lys799Arg(p.K799R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51784408:51784408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3019G>A |
| AA Mutation | p.Val1007Ile(p.V1007I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790286:51790286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2197C>A |
| AA Mutation | p.Pro733Thr(p.P733T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51789057:51789057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747787961 |
| CDS Mutation | c.2546C>T |
| AA Mutation | p.Ser849Leu(p.S849L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791908:51791908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.575C>T |
| AA Mutation | p.Ala192Val(p.A192V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217086 |
| Start | 51792301:51792301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.182C>T |
| AA Mutation | p.Ala61Val(p.A61V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791346:51791346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1137C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790332:51790332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2151G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217086 |
| Start | 51788939:51788939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11698418 |
| CDS Mutation | c.2664C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791487:51791487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137963401 |
| CDS Mutation | c.996C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217086 |
| Start | 51802352:51802352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.57C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217086 |
| Start | 51784397:51784397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748658171 |
| CDS Mutation | c.3030C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790344:51790344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2139C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217086 |
| Start | 51791382:51791382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773682459 |
| CDS Mutation | c.1101C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217086 |
| Start | 51790634:51790634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1849C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000217086 |
| Start | 51784444:51784444(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs753320334 |
| CDS Mutation | c.2983delG |
| AA Mutation | p.Val995PhefsTer14(p.V995Ffs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000217086 |
| Start | 51791192:51791192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1291C>T |
| AA Mutation | p.Arg431Ter(p.R431*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000217086 |
| Start | 51784443:51784444(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs765680621 |
| CDS Mutation | c.2983dupG |
| AA Mutation | p.Val995GlyfsTer16(p.V995Gfs*16) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |