Primary Site >> Stomach Cancer
Gene >> CACNA1E
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181737628:181737628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3526G>A |
| AA Mutation | p.Val1176Ile(p.V1176I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181762607:181762607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4639T>C |
| AA Mutation | p.Phe1547Leu(p.F1547L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181763461:181763461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4745G>A |
| AA Mutation | p.Arg1582His(p.R1582H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181772181:181772181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5089G>T |
| AA Mutation | p.Asp1697Tyr(p.D1697Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181757999:181757999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4382C>T |
| AA Mutation | p.Pro1461Leu(p.P1461L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181651386:181651386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1000C>A |
| AA Mutation | p.Leu334Ile(p.L334I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181651377:181651377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.991T>G |
| AA Mutation | p.Phe331Val(p.F331V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181772103:181772103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5011T>C |
| AA Mutation | p.Ser1671Pro(p.S1671P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181732953:181732953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2867G>A |
| AA Mutation | p.Gly956Glu(p.G956E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181717252:181717252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1475G>A |
| AA Mutation | p.Cys492Tyr(p.C492Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181763497:181763497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4781G>A |
| AA Mutation | p.Arg1594His(p.R1594H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181715382:181715382(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1216G>A |
| AA Mutation | p.Ala406Thr(p.A406T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181580675:181580675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.850G>A |
| AA Mutation | p.Gly284Ser(p.G284S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181732899:181732899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762485881 |
| CDS Mutation | c.2813G>A |
| AA Mutation | p.Arg938Gln(p.R938Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181794990:181794990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768597410 |
| CDS Mutation | c.6154C>T |
| AA Mutation | p.Arg2052Trp(p.R2052W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367573 |
| Start | 181755237:181755237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3829G>A |
| AA Mutation | p.Ala1277Thr(p.A1277T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181772170:181772170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5078G>A |
| AA Mutation | p.Arg1693His(p.R1693H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181737614:181737614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3512C>T |
| AA Mutation | p.Ala1171Val(p.A1171V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181757959:181757959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4342G>A |
| AA Mutation | p.Asp1448Asn(p.D1448N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798749:181798749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749565023 |
| CDS Mutation | c.6857G>A |
| AA Mutation | p.Arg2286Gln(p.R2286Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181577803:181577803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140645319 |
| CDS Mutation | c.550G>A |
| AA Mutation | p.Val184Met(p.V184M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181483937:181483937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.193G>A |
| AA Mutation | p.Val65Ile(p.V65I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798488:181798488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6596C>A |
| AA Mutation | p.Ala2199Asp(p.A2199D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798530:181798530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6638C>A |
| AA Mutation | p.Ser2213Tyr(p.S2213Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181755385:181755385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3977A>G |
| AA Mutation | p.Glu1326Gly(p.E1326G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181752223:181752223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3812G>A |
| AA Mutation | p.Arg1271His(p.R1271H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181580642:181580642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.817T>G |
| AA Mutation | p.Cys273Gly(p.C273G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798542:181798542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6650A>G |
| AA Mutation | p.Gln2217Arg(p.Q2217R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181794919:181794919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6083G>A |
| AA Mutation | p.Arg2028His(p.R2028H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181762613:181762613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4645A>G |
| AA Mutation | p.Thr1549Ala(p.T1549A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181726156:181726156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776757923 |
| CDS Mutation | c.2234C>T |
| AA Mutation | p.Ser745Leu(p.S745L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181785735:181785735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747480727 |
| CDS Mutation | c.5702G>A |
| AA Mutation | p.Arg1901His(p.R1901H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181733636:181733636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3148G>A |
| AA Mutation | p.Glu1050Lys(p.E1050K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181798508:181798508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6616T>C |
| AA Mutation | p.Cys2206Arg(p.C2206R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181737575:181737575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3473G>A |
| AA Mutation | p.Cys1158Tyr(p.C1158Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181651374:181651374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.988T>C |
| AA Mutation | p.Tyr330His(p.Y330H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181752184:181752184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3773G>A |
| AA Mutation | p.Arg1258Gln(p.R1258Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181758026:181758026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4409G>A |
| AA Mutation | p.Arg1470His(p.R1470H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181758028:181758028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4411G>A |
| AA Mutation | p.Val1471Met(p.V1471M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181755327:181755327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373085902 |
| CDS Mutation | c.3919G>A |
| AA Mutation | p.Ala1307Thr(p.A1307T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181736393:181736393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3381G>A |
| AA Mutation | p.Met1127Ile(p.M1127I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181758849:181758849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4586T>C |
| AA Mutation | p.Val1529Ala(p.V1529A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181732845:181732845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377338098 |
| CDS Mutation | c.2759G>A |
| AA Mutation | p.Arg920His(p.R920H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367573 |
| Start | 181737646:181737646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3544C>T |
| AA Mutation | p.Arg1182Cys(p.R1182C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181737606:181737606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746010047 |
| CDS Mutation | c.3504C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181737615:181737615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565145928 |
| CDS Mutation | c.3513G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181755293:181755293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3885G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181755314:181755314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3906C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181794986:181794986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6150T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181724519:181724519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372607441 |
| CDS Mutation | c.2124C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181483870:181483870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761296841 |
| CDS Mutation | c.126G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181721853:181721853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2052T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367573 |
| Start | 181756946:181756946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530293956 |
| CDS Mutation | c.4149T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |