Primary Site >> Stomach Cancer
Gene >> MFRP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449574 |
| Start | 119341969:119341969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1403C>A |
| AA Mutation | p.Pro468His(p.P468H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449574 |
| Start | 119345854:119345854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.346A>C |
| AA Mutation | p.Thr116Pro(p.T116P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449574 |
| Start | 119345506:119345506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.555G>T |
| AA Mutation | p.Lys185Asn(p.K185N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449574 |
| Start | 119346323:119346323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.106C>T |
| AA Mutation | p.Pro36Ser(p.P36S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449574 |
| Start | 119346501:119346501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13T>C |
| AA Mutation | p.Ser5Pro(p.S5P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449574 |
| Start | 119341603:119341603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1685T>C |
| AA Mutation | p.Phe562Ser(p.F562S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449574 |
| Start | 119343898:119343898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1042C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449574 |
| Start | 119345443:119345443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.618T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449574 |
| Start | 119341692:119341692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1596C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449574 |
| Start | 119342964:119342964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764605750 |
| CDS Mutation | c.1164G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000449574 |
| Start | 119342978:119342978(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs757712621 |
| CDS Mutation | c.1150delC |
| AA Mutation | p.His384ThrfsTer94(p.H384Tfs*94) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000449574 |
| Start | 119345563:119345563(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs587776596 |
| CDS Mutation | c.498delC |
| AA Mutation | p.Asn167ThrfsTer25(p.N167Tfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000449574 |
| Start | 119344980:119344980(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.666delC |
| AA Mutation | p.Thr223ArgfsTer83(p.T223Rfs*83) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000449574 |
| Start | 119345562:119345563(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs606231145 |
| CDS Mutation | c.498dupC |
| AA Mutation | p.Asn167GlnfsTer34(p.N167Qfs*34) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |