Primary Site >> Stomach Cancer
Gene >> FMNL3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335154 |
| Start | 49662042:49662042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752076456 |
| CDS Mutation | c.376C>T |
| AA Mutation | p.Arg126Trp(p.R126W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335154 |
| Start | 49647722:49647722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779542588 |
| CDS Mutation | c.2759G>A |
| AA Mutation | p.Arg920Gln(p.R920Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335154 |
| Start | 49650712:49650712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1964G>A |
| AA Mutation | p.Gly655Asp(p.G655D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335154 |
| Start | 49650773:49650773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1903A>G |
| AA Mutation | p.Lys635Glu(p.K635E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335154 |
| Start | 49645877:49645877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545464076 |
| CDS Mutation | c.3022C>T |
| AA Mutation | p.Arg1008Cys(p.R1008C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335154 |
| Start | 49658493:49658493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762982824 |
| CDS Mutation | c.554C>T |
| AA Mutation | p.Ser185Leu(p.S185L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335154 |
| Start | 49652001:49652001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1535C>T |
| AA Mutation | p.Pro512Leu(p.P512L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335154 |
| Start | 49654265:49654265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998C>T |
| AA Mutation | p.Ser333Leu(p.S333L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335154 |
| Start | 49649516:49649516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764301507 |
| CDS Mutation | c.2258C>T |
| AA Mutation | p.Ala753Val(p.A753V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335154 |
| Start | 49648212:49648212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759869506 |
| CDS Mutation | c.2657G>A |
| AA Mutation | p.Arg886Gln(p.R886Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335154 |
| Start | 49658459:49658459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749638078 |
| CDS Mutation | c.588G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335154 |
| Start | 49648199:49648199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374343899 |
| CDS Mutation | c.2670G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335154 |
| Start | 49649518:49649518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751577308 |
| CDS Mutation | c.2256G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000335154 |
| Start | 49651287:49651287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773386245 |
| CDS Mutation | c.1678C>T |
| AA Mutation | p.Arg560Ter(p.R560*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000335154 |
| Start | 49654960:49654961(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.909dupT |
| AA Mutation | p.Glu304Ter(p.E304*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |