Primary Site >> Stomach Cancer
Gene >> TIMP3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266085 |
| Start | 32849524:32849524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.194A>G |
| AA Mutation | p.Lys65Arg(p.K65R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266085 |
| Start | 32858098:32858098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.398A>C |
| AA Mutation | p.Lys133Thr(p.K133T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266085 |
| Start | 32849480:32849480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.150G>C |
| AA Mutation | p.Lys50Asn(p.K50N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266085 |
| Start | 32857301:32857301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.257C>A |
| AA Mutation | p.Ala86Asp(p.A86D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266085 |
| Start | 32849506:32849506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779515006 |
| CDS Mutation | c.176C>T |
| AA Mutation | p.Thr59Met(p.T59M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000266085 |
| Start | 32858094:32858094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.394C>T |
| AA Mutation | p.Arg132Cys(p.R132C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000266085 |
| Start | 32859337:32859337(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.602delC |
| AA Mutation | p.Pro201ArgfsTer26(p.P201Rfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000266085 |
| Start | 32859336:32859337(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs749890843 |
| CDS Mutation | c.602dupC |
| AA Mutation | p.Asp202GlyfsTer2(p.D202Gfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |