Primary Site >> Stomach Cancer
Gene >> TGM4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296125 |
| Start | 44903952:44903952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1040A>G |
| AA Mutation | p.Gln347Arg(p.Q347R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296125 |
| Start | 44901802:44901802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377171248 |
| CDS Mutation | c.842C>T |
| AA Mutation | p.Ala281Val(p.A281V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296125 |
| Start | 44890702:44890702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.400C>A |
| AA Mutation | p.Leu134Ile(p.L134I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296125 |
| Start | 44901819:44901819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781223579 |
| CDS Mutation | c.859C>T |
| AA Mutation | p.Arg287Cys(p.R287C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296125 |
| Start | 44907173:44907173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1300A>G |
| AA Mutation | p.Ile434Val(p.I434V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296125 |
| Start | 44901628:44901628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.762G>T |
| AA Mutation | p.Gln254His(p.Q254H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296125 |
| Start | 44901807:44901807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.847G>T |
| AA Mutation | p.Gly283Cys(p.G283C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296125 |
| Start | 44911284:44911284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1791C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296125 |
| Start | 44910352:44910352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528006561 |
| CDS Mutation | c.1590G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296125 |
| Start | 44887693:44887693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777957841 |
| CDS Mutation | c.198G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000296125 |
| Start | 44901590:44901591(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.728dupC |
| AA Mutation | p.Tyr244IlefsTer67(p.Y244Ifs*67) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |