Primary Site >> Stomach Cancer
Gene >> LTF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46448988:46448988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763164407 |
| CDS Mutation | c.1087C>T |
| AA Mutation | p.Arg363Trp(p.R363W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46449943:46449943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.968C>T |
| AA Mutation | p.Ala323Val(p.A323V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46459718:46459718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776865450 |
| CDS Mutation | c.145C>T |
| AA Mutation | p.Arg49Cys(p.R49C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46441458:46441458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762422805 |
| CDS Mutation | c.1681G>A |
| AA Mutation | p.Val561Ile(p.V561I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46443477:46443477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs193150262 |
| CDS Mutation | c.1619G>A |
| AA Mutation | p.Ser540Asn(p.S540N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46448913:46448913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1162G>A |
| AA Mutation | p.Val388Met(p.V388M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46446481:46446481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1316G>T |
| AA Mutation | p.Ser439Ile(p.S439I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46456298:46456298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.308C>A |
| AA Mutation | p.Thr103Asn(p.T103N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46448918:46448918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1157G>A |
| AA Mutation | p.Gly386Asp(p.G386D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000231751 |
| Start | 46459657:46459657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765686239 |
| CDS Mutation | c.206C>T |
| AA Mutation | p.Ala69Val(p.A69V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46439325:46439325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188531064 |
| CDS Mutation | c.1879C>T |
| AA Mutation | p.Arg627Cys(p.R627C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000231751 |
| Start | 46456388:46456388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.218C>T |
| AA Mutation | p.Ala73Val(p.A73V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000231751 |
| Start | 46456303:46456303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145234336 |
| CDS Mutation | c.303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000231751 |
| Start | 46439419:46439419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267599843 |
| CDS Mutation | c.1785C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000231751 |
| Start | 46443488:46443488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376334318 |
| CDS Mutation | c.1608C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000231751 |
| Start | 46438106:46438106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1932T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |