Primary Site >> Stomach Cancer
Gene >> MMP10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000279441 |
| Start | 102779507:102779507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.344A>G |
| AA Mutation | p.Tyr115Cys(p.Y115C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000279441 |
| Start | 102776352:102776352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754542564 |
| CDS Mutation | c.860C>T |
| AA Mutation | p.Ala287Val(p.A287V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000279441 |
| Start | 102772917:102772917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1156A>G |
| AA Mutation | p.Lys386Glu(p.K386E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000279441 |
| Start | 102779592:102779592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.259C>T |
| AA Mutation | p.Arg87Cys(p.R87C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000279441 |
| Start | 102779744:102779744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.107A>G |
| AA Mutation | p.Gln36Arg(p.Q36R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000279441 |
| Start | 102776415:102776415(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.797delC |
| AA Mutation | p.Pro266LeufsTer36(p.P266Lfs*36) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000279441 |
| Start | 102779664:102779664(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.187delA |
| AA Mutation | p.Ile63SerfsTer12(p.I63Sfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000279441 |
| Start | 102776303:102776304(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.908dupG |
| AA Mutation | p.Glu304ArgfsTer6(p.E304Rfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000279441 |
| Start | 102779663:102779664(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs746110396 |
| CDS Mutation | c.187dupA |
| AA Mutation | p.Ile63AsnfsTer19(p.I63Nfs*19) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |