Primary Site >> Stomach Cancer
Gene >> FBLN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327858 |
| Start | 45574635:45574635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1822G>A |
| AA Mutation | p.Glu608Lys(p.E608K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327858 |
| Start | 45600316:45600316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369461467 |
| CDS Mutation | c.1982G>A |
| AA Mutation | p.Arg661His(p.R661H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327858 |
| Start | 45577085:45577085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775498492 |
| CDS Mutation | c.1949G>A |
| AA Mutation | p.Arg650His(p.R650H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327858 |
| Start | 45600324:45600324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1990C>T |
| AA Mutation | p.Arg664Trp(p.R664W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327858 |
| Start | 45518714:45518714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs573352225 |
| CDS Mutation | c.112G>A |
| AA Mutation | p.Ala38Thr(p.A38T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327858 |
| Start | 45550536:45550536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141938890 |
| CDS Mutation | c.1618G>A |
| AA Mutation | p.Glu540Lys(p.E540K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327858 |
| Start | 45548663:45548663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1492T>C |
| AA Mutation | p.Cys498Arg(p.C498R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327858 |
| Start | 45533114:45533114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.596G>T |
| AA Mutation | p.Cys199Phe(p.C199F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327858 |
| Start | 45550580:45550580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1662C>A |
| AA Mutation | p.Phe554Leu(p.F554L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327858 |
| Start | 45574611:45574611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149912059 |
| CDS Mutation | c.1798G>A |
| AA Mutation | p.Val600Ile(p.V600I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327858 |
| Start | 45574577:45574577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1764C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327858 |
| Start | 45543408:45543408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201140780 |
| CDS Mutation | c.1203C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327858 |
| Start | 45527903:45527903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144410933 |
| CDS Mutation | c.378C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327858 |
| Start | 45533088:45533088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.570C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327858 |
| Start | 45541362:45541362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376616186 |
| CDS Mutation | c.1056G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327858 |
| Start | 45542207:45542207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199835399 |
| CDS Mutation | c.1119C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |