Primary Site >> Stomach Cancer
Gene >> SOX10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360880 |
| Start | 37977915:37977915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649C>A |
| AA Mutation | p.Pro217Thr(p.P217T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360880 |
| Start | 37973815:37973815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770105416 |
| CDS Mutation | c.1081G>A |
| AA Mutation | p.Ala361Thr(p.A361T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360880 |
| Start | 37973607:37973607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1289C>T |
| AA Mutation | p.Pro430Leu(p.P430L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360880 |
| Start | 37977990:37977990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.574G>T |
| AA Mutation | p.Gly192Cys(p.G192C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360880 |
| Start | 37973818:37973818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1078A>G |
| AA Mutation | p.Thr360Ala(p.T360A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360880 |
| Start | 37983505:37983505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.280G>A |
| AA Mutation | p.Val94Ile(p.V94I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360880 |
| Start | 37983508:37983508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.277C>T |
| AA Mutation | p.Arg93Cys(p.R93C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360880 |
| Start | 37974118:37974118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367743809 |
| CDS Mutation | c.778G>A |
| AA Mutation | p.Gly260Arg(p.G260R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360880 |
| Start | 37983392:37983392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.393C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360880 |
| Start | 37973948:37973948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754568838 |
| CDS Mutation | c.948C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360880 |
| Start | 37977937:37977937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.627C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360880 |
| Start | 37977964:37977964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143057951 |
| CDS Mutation | c.600C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |