Primary Site >> Liver Cancer
Gene >> LAMA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6949124:6949124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8533T>C |
| AA Mutation | p.Tyr2845His(p.Y2845H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7023226:7023226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2639C>A |
| AA Mutation | p.Ala880Asp(p.A880D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7033067:7033067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2080A>T |
| AA Mutation | p.Ser694Cys(p.S694C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7008567:7008567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4043A>G |
| AA Mutation | p.Lys1348Arg(p.K1348R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6975956:6975956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6470A>T |
| AA Mutation | p.Tyr2157Phe(p.Y2157F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6958591:6958591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751200271 |
| CDS Mutation | c.7850C>T |
| AA Mutation | p.Thr2617Met(p.T2617M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000389658 |
| Start | 6993752:6993752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4897C>T |
| AA Mutation | p.Leu1633Phe(p.L1633F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6978216:6978216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6170T>A |
| AA Mutation | p.Leu2057Gln(p.L2057Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7080343:7080343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375547281 |
| CDS Mutation | c.176G>A |
| AA Mutation | p.Arg59Gln(p.R59Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6985310:6985310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532071998 |
| CDS Mutation | c.5587A>T |
| AA Mutation | p.Asn1863Tyr(p.N1863Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7017349:7017349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2737G>T |
| AA Mutation | p.Val913Leu(p.V913L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7016514:7016514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2966C>A |
| AA Mutation | p.Ala989Asp(p.A989D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6985273:6985273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5624C>G |
| AA Mutation | p.Ala1875Gly(p.A1875G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7013888:7013888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3290C>A |
| AA Mutation | p.Thr1097Lys(p.T1097K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6955381:6955381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8179C>T |
| AA Mutation | p.Pro2727Ser(p.P2727S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389658 |
| Start | 6956654:6956654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8076A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389658 |
| Start | 7016606:7016606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199612213 |
| CDS Mutation | c.2874C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389658 |
| Start | 7013923:7013923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375804587 |
| CDS Mutation | c.3255C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389658 |
| Start | 6956645:6956645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8085G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389658 |
| Start | 6958646:6958646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7795T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389658 |
| Start | 7002350:7002350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4296T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389658 |
| Start | 7026083:7026083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2298C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389658 |
| Start | 7008503:7008503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374423781 |
| CDS Mutation | c.4107G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389658 |
| Start | 6942223:6942223(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.9084delA |
| AA Mutation | p.Lys3028AsnfsTer13(p.K3028Nfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000389658 |
| Start | 6956709:6956709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8021G>A |
| AA Mutation | p.Trp2674Ter(p.W2674*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | splice_donor_variant;coding_sequence_variant;intron_variant |
| Transcription ID | ENST00000389658 |
| Start | 6965285:6965307(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7176_7195+3delCCAGCGAAACCGGAAGCAAGGTA |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |