Primary Site >> Stomach Cancer
Gene >> COL10A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243222 |
| Start | 116121641:116121641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.475G>A |
| AA Mutation | p.Gly159Arg(p.G159R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243222 |
| Start | 116121352:116121352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.764C>T |
| AA Mutation | p.Pro255Leu(p.P255L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243222 |
| Start | 116120246:116120246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1870A>G |
| AA Mutation | p.Thr624Ala(p.T624A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243222 |
| Start | 116120354:116120354(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1762A>C |
| AA Mutation | p.Ile588Leu(p.I588L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243222 |
| Start | 116121722:116121722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.394G>A |
| AA Mutation | p.Ala132Thr(p.A132T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243222 |
| Start | 116120816:116120816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778701685 |
| CDS Mutation | c.1300G>A |
| AA Mutation | p.Gly434Arg(p.G434R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000243222 |
| Start | 116125363:116125363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.130A>G |
| AA Mutation | p.Ile44Val(p.I44V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243222 |
| Start | 116121726:116121726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.390A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243222 |
| Start | 116121654:116121654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777052338 |
| CDS Mutation | c.462G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243222 |
| Start | 116120844:116120844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749839210 |
| CDS Mutation | c.1272G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000243222 |
| Start | 116121192:116121192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374250798 |
| CDS Mutation | c.924A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243222 |
| Start | 116120587:116120587(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1529delC |
| AA Mutation | p.Pro510LeufsTer17(p.P510Lfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000243222 |
| Start | 116121589:116121589(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.527delA |
| AA Mutation | p.Lys176ArgfsTer9(p.K176Rfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |