Primary Site >> Stomach Cancer
Gene >> FLII
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327031 |
| Start | 18252037:18252037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775990658 |
| CDS Mutation | c.1208C>T |
| AA Mutation | p.Ala403Val(p.A403V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327031 |
| Start | 18245150:18245150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3798G>T |
| AA Mutation | p.Lys1266Asn(p.K1266N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327031 |
| Start | 18247740:18247740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2404A>G |
| AA Mutation | p.Lys802Glu(p.K802E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327031 |
| Start | 18251462:18251462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1399C>G |
| AA Mutation | p.Arg467Gly(p.R467G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327031 |
| Start | 18251288:18251288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1573G>A |
| AA Mutation | p.Ala525Thr(p.A525T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327031 |
| Start | 18254833:18254833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.349A>G |
| AA Mutation | p.Thr117Ala(p.T117A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327031 |
| Start | 18245230:18245230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563225941 |
| CDS Mutation | c.3718C>T |
| AA Mutation | p.Arg1240Cys(p.R1240C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327031 |
| Start | 18253377:18253377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.937A>G |
| AA Mutation | p.Ile313Val(p.I313V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327031 |
| Start | 18251330:18251330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1531C>T |
| AA Mutation | p.Pro511Ser(p.P511S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327031 |
| Start | 18253454:18253454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.860C>T |
| AA Mutation | p.Ala287Val(p.A287V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327031 |
| Start | 18245192:18245192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547009769 |
| CDS Mutation | c.3756C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |