Primary Site >> Stomach Cancer
Gene >> MPG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219431 |
| Start | 85494:85494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.614C>A |
| AA Mutation | p.Ala205Asp(p.A205D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219431 |
| Start | 83170:83170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764172082 |
| CDS Mutation | c.434G>A |
| AA Mutation | p.Arg145His(p.R145H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219431 |
| Start | 85515:85515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142373562 |
| CDS Mutation | c.635G>A |
| AA Mutation | p.Arg212His(p.R212H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219431 |
| Start | 79491:79491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373341989 |
| CDS Mutation | c.106G>A |
| AA Mutation | p.Asp36Asn(p.D36N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219431 |
| Start | 79445:79445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.60A>T |
| AA Mutation | p.Gln20His(p.Q20H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219431 |
| Start | 79487:79487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754765496 |
| CDS Mutation | c.102G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000219431 |
| Start | 79444:79444(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.62delA |
| AA Mutation | p.Lys21ArgfsTer87(p.K21Rfs*87) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |