Primary Site >> Liver Cancer
Gene >> FN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215384940:215384940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4376C>A |
| AA Mutation | p.Ala1459Glu(p.A1459E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215394703:215394703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3621A>T |
| AA Mutation | p.Arg1207Ser(p.R1207S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215408328:215408328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2398A>G |
| AA Mutation | p.Ser800Gly(p.S800G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215397178:215397178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3563C>A |
| AA Mutation | p.Thr1188Asn(p.T1188N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215397188:215397188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746992481 |
| CDS Mutation | c.3553A>G |
| AA Mutation | p.Asn1185Asp(p.N1185D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215379173:215379173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5306A>T |
| AA Mutation | p.Asn1769Ile(p.N1769I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215391658:215391658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3953C>A |
| AA Mutation | p.Pro1318His(p.P1318H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215434800:215434800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.173A>G |
| AA Mutation | p.His58Arg(p.H58R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215383451:215383451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140153061 |
| CDS Mutation | c.4654G>A |
| AA Mutation | p.Asp1552Asn(p.D1552N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215362073:215362073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759273898 |
| CDS Mutation | c.6985C>T |
| AA Mutation | p.Arg2329Cys(p.R2329C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359671 |
| Start | 215406373:215406373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772017194 |
| CDS Mutation | c.2851G>A |
| AA Mutation | p.Gly951Arg(p.G951R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359671 |
| Start | 215376508:215376508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5604C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359671 |
| Start | 215397189:215397189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3552A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359671 |
| Start | 215434787:215434790(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.183_186delAAAT |
| AA Mutation | p.Gln63SerfsTer7(p.Q63Sfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359671 |
| Start | 215384089:215384090(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.4551dupT |
| AA Mutation | p.Val1518CysfsTer20(p.V1518Cfs*20) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000359671 |
| Start | 215373321:215373321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111852829 |
| CDS Mutation | c.5974+1G>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |