Primary Site >> Stomach Cancer
Gene >> CTSD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236671 |
| Start | 1757454:1757454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767282477 |
| CDS Mutation | c.574G>A |
| AA Mutation | p.Ala192Thr(p.A192T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236671 |
| Start | 1753637:1753637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1105G>A |
| AA Mutation | p.Gly369Ser(p.G369S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236671 |
| Start | 1757363:1757363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665A>G |
| AA Mutation | p.Lys222Arg(p.K222R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000236671 |
| Start | 1759063:1759063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.377A>C |
| AA Mutation | p.Asp126Ala(p.D126A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000236671 |
| Start | 1759607:1759607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372181453 |
| CDS Mutation | c.261G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000236671 |
| Start | 1753665:1753665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138940129 |
| CDS Mutation | c.1077G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000236671 |
| Start | 1753997:1753997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774332555 |
| CDS Mutation | c.969C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000236671 |
| Start | 1754090:1754090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.876C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000236671 |
| Start | 1754917:1754917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.816C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000236671 |
| Start | 1759600:1759600(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.268delC |
| AA Mutation | p.Gln90SerfsTer43(p.Q90Sfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000236671 |
| Start | 1759599:1759600(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs752612332 |
| CDS Mutation | c.268dupC |
| AA Mutation | p.Gln90ProfsTer50(p.Q90Pfs*50) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |