Primary Site >> Stomach Cancer
Gene >> FMNL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45243298:45243298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377137839 |
| CDS Mutation | c.2191C>T |
| AA Mutation | p.Arg731Cys(p.R731C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45237291:45237291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.734G>A |
| AA Mutation | p.Ser245Asn(p.S245N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000331495 |
| Start | 45232369:45232369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.216G>T |
| AA Mutation | p.Glu72Asp(p.E72D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45244197:45244197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2470G>A |
| AA Mutation | p.Ala824Thr(p.A824T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45245412:45245412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2888C>T |
| AA Mutation | p.Ala963Val(p.A963V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45239013:45239013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1028G>A |
| AA Mutation | p.Arg343His(p.R343H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45237311:45237311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.754G>A |
| AA Mutation | p.Ala252Thr(p.A252T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000331495 |
| Start | 45240477:45240477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1082G>T |
| AA Mutation | p.Arg361Met(p.R361M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45243299:45243299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749913183 |
| CDS Mutation | c.2192G>A |
| AA Mutation | p.Arg731His(p.R731H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45245071:45245071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2691C>A |
| AA Mutation | p.Phe897Leu(p.F897L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45234122:45234122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.536A>G |
| AA Mutation | p.Lys179Arg(p.K179R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45240582:45240582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1187C>T |
| AA Mutation | p.Ala396Val(p.A396V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45245343:45245343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2819T>C |
| AA Mutation | p.Met940Thr(p.M940T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331495 |
| Start | 45238625:45238625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.956A>G |
| AA Mutation | p.Asn319Ser(p.N319S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331495 |
| Start | 45243207:45243207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2100C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331495 |
| Start | 45245015:45245015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2635C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331495 |
| Start | 45243315:45243315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2208T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331495 |
| Start | 45243183:45243183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2076C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331495 |
| Start | 45245661:45245661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2922C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331495 |
| Start | 45241200:45241200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1302C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331495 |
| Start | 45240553:45240553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749865243 |
| CDS Mutation | c.1158G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |