Primary Site >> Stomach Cancer
Gene >> MIP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257979 |
| Start | 56453728:56453728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.388G>A |
| AA Mutation | p.Ala130Thr(p.A130T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000257979 |
| Start | 56453074:56453074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.604T>C |
| AA Mutation | p.Trp202Arg(p.W202R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257979 |
| Start | 56451395:56451395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770704370 |
| CDS Mutation | c.677G>A |
| AA Mutation | p.Arg226Gln(p.R226Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257979 |
| Start | 56454571:56454571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758696671 |
| CDS Mutation | c.43G>A |
| AA Mutation | p.Ala15Thr(p.A15T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257979 |
| Start | 56453703:56453703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121917867 |
| CDS Mutation | c.413C>T |
| AA Mutation | p.Thr138Met(p.T138M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257979 |
| Start | 56453632:56453632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.484C>A |
| AA Mutation | p.Leu162Met(p.L162M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257979 |
| Start | 56454410:56454410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.204T>G |
| AA Mutation | p.Asn68Lys(p.N68K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257979 |
| Start | 56453692:56453692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.424G>A |
| AA Mutation | p.Val142Met(p.V142M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257979 |
| Start | 56453702:56453702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746222267 |
| CDS Mutation | c.414G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257979 |
| Start | 56453744:56453744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141768870 |
| CDS Mutation | c.372G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257979 |
| Start | 56453082:56453083(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.595_596delAC |
| AA Mutation | p.Thr199Ter(p.T199*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |