Primary Site >> Stomach Cancer
Gene >> TGM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206765 |
| Start | 24255405:24255405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1604A>T |
| AA Mutation | p.Asn535Ile(p.N535I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206765 |
| Start | 24255490:24255490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200829531 |
| CDS Mutation | c.1519C>T |
| AA Mutation | p.Arg507Trp(p.R507W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206765 |
| Start | 24258607:24258607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1226C>T |
| AA Mutation | p.Thr409Ile(p.T409I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206765 |
| Start | 24261809:24261809(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs2229462 |
| CDS Mutation | c.394G>A |
| AA Mutation | p.Asp132Asn(p.D132N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206765 |
| Start | 24255223:24255223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1676C>T |
| AA Mutation | p.Thr559Ile(p.T559I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206765 |
| Start | 24258592:24258592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1241A>G |
| AA Mutation | p.Asp414Gly(p.D414G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000206765 |
| Start | 24254687:24254687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754059368 |
| CDS Mutation | c.2065C>T |
| AA Mutation | p.Arg689Cys(p.R689C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000206765 |
| Start | 24261795:24261795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142338588 |
| CDS Mutation | c.408C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000206765 |
| Start | 24255249:24255249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1650A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000206765 |
| Start | 24260670:24260670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757301708 |
| CDS Mutation | c.537G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000206765 |
| Start | 24249502:24249502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2265G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000206765 |
| Start | 24261792:24261792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145002586 |
| CDS Mutation | c.411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000206765 |
| Start | 24249404:24249404(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2363delC |
| AA Mutation | p.Pro788GlnfsTer18(p.P788Qfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000206765 |
| Start | 24260640:24260641(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.566dupG |
| AA Mutation | p.Ser190GlnfsTer49(p.S190Qfs*49) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |