Primary Site >> Stomach Cancer
Gene >> SOX7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726140:10726140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.765C>A |
| AA Mutation | p.His255Gln(p.H255Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10730287:10730287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.147G>T |
| AA Mutation | p.Met49Ile(p.M49I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10725886:10725886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150061334 |
| CDS Mutation | c.1019G>A |
| AA Mutation | p.Gly340Asp(p.G340D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726522:10726522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778831845 |
| CDS Mutation | c.383G>A |
| AA Mutation | p.Arg128His(p.R128H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726645:10726645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.260C>T |
| AA Mutation | p.Thr87Met(p.T87M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726248:10726248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370342985 |
| CDS Mutation | c.657C>A |
| AA Mutation | p.Phe219Leu(p.F219L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726403:10726403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.502G>A |
| AA Mutation | p.Gly168Ser(p.G168S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10725919:10725919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370726272 |
| CDS Mutation | c.986G>A |
| AA Mutation | p.Arg329His(p.R329H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726622:10726622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.283G>A |
| AA Mutation | p.Val95Met(p.V95M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726624:10726624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.281A>G |
| AA Mutation | p.Tyr94Cys(p.Y94C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726207:10726207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775918915 |
| CDS Mutation | c.698G>A |
| AA Mutation | p.Arg233His(p.R233H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726651:10726651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765208739 |
| CDS Mutation | c.254C>T |
| AA Mutation | p.Ala85Val(p.A85V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304501 |
| Start | 10725771:10725771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755524110 |
| CDS Mutation | c.1134G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726047:10726047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753879424 |
| CDS Mutation | c.858G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304501 |
| Start | 10725990:10725990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.915G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726182:10726182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.723G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726136:10726136(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.769delC |
| AA Mutation | p.Leu257TrpfsTer14(p.L257Wfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726442:10726442(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs774544038 |
| CDS Mutation | c.463delG |
| AA Mutation | p.Ala155ArgfsTer116(p.A155Rfs*116) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726183:10726183(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.722delC |
| AA Mutation | p.Pro241ArgfsTer30(p.P241Rfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000304501 |
| Start | 10726441:10726442(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs769092194 |
| CDS Mutation | c.463dupG |
| AA Mutation | p.Ala155GlyfsTer10(p.A155Gfs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |