Primary Site >> Stomach Cancer
Gene >> FOXN2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340553 |
| Start | 48375258:48375258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1111C>T |
| AA Mutation | p.Pro371Ser(p.P371S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340553 |
| Start | 48346577:48346577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.363T>G |
| AA Mutation | p.Ile121Met(p.I121M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340553 |
| Start | 48374927:48374927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.780G>T |
| AA Mutation | p.Lys260Asn(p.K260N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000340553 |
| Start | 48375310:48375310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1163A>G |
| AA Mutation | p.Gln388Arg(p.Q388R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340553 |
| Start | 48375104:48375104(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778517201 |
| CDS Mutation | c.957C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340553 |
| Start | 48375374:48375374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1227A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000340553 |
| Start | 48375281:48375281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1134A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000340553 |
| Start | 48374953:48374953(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.812delA |
| AA Mutation | p.Lys271ArgfsTer22(p.K271Rfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000340553 |
| Start | 48346528:48346528(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.321delA |
| AA Mutation | p.Lys107AsnfsTer60(p.K107Nfs*60) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000340553 |
| Start | 48362695:48362695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138143881 |
| CDS Mutation | c.691C>T |
| AA Mutation | p.Arg231Ter(p.R231*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |