Primary Site >> Liver Cancer
Gene >> CACNA1E
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798748:181798748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762766720 |
| CDS Mutation | c.6856C>T |
| AA Mutation | p.Arg2286Trp(p.R2286W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181731215:181731215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2281C>A |
| AA Mutation | p.Pro761Thr(p.P761T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181711031:181711031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs575157426 |
| CDS Mutation | c.1133G>A |
| AA Mutation | p.Arg378His(p.R378H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181724496:181724496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2101A>G |
| AA Mutation | p.Ile701Val(p.I701V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181736326:181736326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3314G>T |
| AA Mutation | p.Arg1105Ile(p.R1105I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181510575:181510575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369308237 |
| CDS Mutation | c.365G>A |
| AA Mutation | p.Arg122Gln(p.R122Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181483856:181483856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.112G>T |
| AA Mutation | p.Ala38Ser(p.A38S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181711022:181711022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1124A>T |
| AA Mutation | p.Gln375Leu(p.Q375L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798464:181798464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6572A>T |
| AA Mutation | p.Glu2191Val(p.E2191V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798599:181798599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781574328 |
| CDS Mutation | c.6707A>G |
| AA Mutation | p.His2236Arg(p.H2236R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181756000:181756000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4034G>T |
| AA Mutation | p.Gly1345Val(p.G1345V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181757023:181757023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4226T>C |
| AA Mutation | p.Val1409Ala(p.V1409A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181732735:181732735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2649G>T |
| AA Mutation | p.Trp883Cys(p.W883C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181756036:181756036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4070A>G |
| AA Mutation | p.Asn1357Ser(p.N1357S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798323:181798323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6431C>T |
| AA Mutation | p.Pro2144Leu(p.P2144L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181732491:181732491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2405C>A |
| AA Mutation | p.Ala802Glu(p.A802E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181755300:181755300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3892C>G |
| AA Mutation | p.Leu1298Val(p.L1298V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181732639:181732639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2553C>A |
| AA Mutation | p.Ser851Arg(p.S851R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367573 |
| Start | 181733750:181733750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3262A>T |
| AA Mutation | p.Ile1088Phe(p.I1088F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181784725:181784725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5535C>A |
| AA Mutation | p.His1845Gln(p.H1845Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181724484:181724484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2089G>T |
| AA Mutation | p.Val697Leu(p.V697L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181718102:181718102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1573C>A |
| AA Mutation | p.Leu525Met(p.L525M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181579219:181579219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.764A>T |
| AA Mutation | p.Asn255Ile(p.N255I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181719775:181719775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1663G>A |
| AA Mutation | p.Val555Met(p.V555M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181772175:181772175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5083G>A |
| AA Mutation | p.Gly1695Ser(p.G1695S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181737546:181737546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3444C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181510513:181510513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.303C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181785763:181785763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5730G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798381:181798381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377180948 |
| CDS Mutation | c.6489G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181720831:181720831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1932T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181736309:181736309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3297G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181796705:181796705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778131872 |
| CDS Mutation | c.6246G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367573 |
| Start | 181756057:181756057(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4093delC |
| AA Mutation | p.Leu1365SerfsTer18(p.L1365Sfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000367573 |
| Start | 181716131:181716131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1315+2T>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |