Primary Site >> Stomach Cancer
Gene >> CACNA1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13452922:13452922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.493T>G |
| AA Mutation | p.Leu165Val(p.L165V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13365436:13365436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665C>T |
| AA Mutation | p.Ala222Val(p.A222V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13308434:13308434(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773414013 |
| CDS Mutation | c.1763G>A |
| AA Mutation | p.Arg588His(p.R588H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13235662:13235662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5019G>C |
| AA Mutation | p.Gln1673His(p.Q1673H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13224765:13224765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5633T>G |
| AA Mutation | p.Leu1878Arg(p.L1878R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13235655:13235655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5026A>G |
| AA Mutation | p.Thr1676Ala(p.T1676A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13212433:13212433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539347883 |
| CDS Mutation | c.6140C>T |
| AA Mutation | p.Pro2047Leu(p.P2047L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13308124:13308124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1909G>T |
| AA Mutation | p.Gly637Cys(p.G637C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13262756:13262756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4067T>C |
| AA Mutation | p.Ile1356Thr(p.I1356T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13299096:13299096(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2537A>G |
| AA Mutation | p.Asp846Gly(p.D846G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13286937:13286937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776628272 |
| CDS Mutation | c.3119C>T |
| AA Mutation | p.Ser1040Leu(p.S1040L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13455111:13455111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764554276 |
| CDS Mutation | c.395G>A |
| AA Mutation | p.Arg132Gln(p.R132Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13257366:13257366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4574G>T |
| AA Mutation | p.Ser1525Ile(p.S1525I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13506046:13506046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.179C>T |
| AA Mutation | p.Ala60Val(p.A60V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13255241:13255241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773209223 |
| CDS Mutation | c.4609G>A |
| AA Mutation | p.Ala1537Thr(p.A1537T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13298920:13298920(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2713G>A |
| AA Mutation | p.Ala905Thr(p.A905T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13317284:13317284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1383G>T |
| AA Mutation | p.Lys461Asn(p.K461N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13253064:13253064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4793G>A |
| AA Mutation | p.Arg1598Gln(p.R1598Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13308127:13308127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1906G>A |
| AA Mutation | p.Gly636Ser(p.G636S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13506067:13506067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.158C>T |
| AA Mutation | p.Ala53Val(p.A53V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13334471:13334471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1105C>T |
| AA Mutation | p.Arg369Trp(p.R369W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360228 |
| Start | 13212450:13212450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6123G>T |
| AA Mutation | p.Lys2041Asn(p.K2041N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13255206:13255206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199854716 |
| CDS Mutation | c.4644G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13214538:13214538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5802C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13299233:13299233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2400C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13300582:13300582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2247T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13261547:13261547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4153C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13303873:13303873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373695561 |
| CDS Mutation | c.1998C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13257536:13257536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557205300 |
| CDS Mutation | c.4404G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13255167:13255167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377082780 |
| CDS Mutation | c.4683C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13212492:13212492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6081C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13359681:13359681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs17846910 |
| CDS Mutation | c.903C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13303879:13303879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1992G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13299101:13299101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761929729 |
| CDS Mutation | c.2532C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13307818:13307818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747730451 |
| CDS Mutation | c.1950C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360228 |
| Start | 13298999:13298999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2634C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360228 |
| Start | 13285169:13285169(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs747879307 |
| CDS Mutation | c.3591delA |
| AA Mutation | p.Glu1198ArgfsTer43(p.E1198Rfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360228 |
| Start | 13262815:13262815(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4008delA |
| AA Mutation | p.Asp1337ThrfsTer34(p.D1337Tfs*34) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360228 |
| Start | 13303826:13303826(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2045delG |
| AA Mutation | p.Gly682AlafsTer15(p.G682Afs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360228 |
| Start | 13212418:13212418(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6155delC |
| AA Mutation | p.Pro2052LeufsTer70(p.P2052Lfs*70) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360228 |
| Start | 13298820:13298820(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2813delG |
| AA Mutation | p.Gly938AlafsTer131(p.G938Afs*131) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000360228 |
| Start | 13283381:13283381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3708C>A |
| AA Mutation | p.Cys1236Ter(p.C1236*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000360228 |
| Start | 13285168:13285169(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | null |
| CDS Mutation | c.3591dupA |
| AA Mutation | p.Glu1198ArgfsTer18(p.E1198Rfs*18) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000360228 |
| Start | 13275849:13275849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587776693 |
| CDS Mutation | c.3989+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |