Primary Site >> Stomach Cancer
Gene >> SCN5A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38609823:38609823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473083 |
| CDS Mutation | c.845G>A |
| AA Mutation | p.Arg282His(p.R282H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38587413:38587413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473160 |
| CDS Mutation | c.2423G>A |
| AA Mutation | p.Arg808His(p.R808H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38606110:38606110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1179C>A |
| AA Mutation | p.Phe393Leu(p.F393L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38554371:38554371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4721A>G |
| AA Mutation | p.Glu1574Gly(p.E1574G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38555699:38555699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4499A>C |
| AA Mutation | p.Lys1500Thr(p.K1500T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38551495:38551495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473283 |
| CDS Mutation | c.4877G>A |
| AA Mutation | p.Arg1626His(p.R1626H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38633228:38633228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473045 |
| CDS Mutation | c.80G>A |
| AA Mutation | p.Arg27His(p.R27H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38550569:38550569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473637 |
| CDS Mutation | c.5803G>A |
| AA Mutation | p.Gly1935Ser(p.G1935S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38603744:38603744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473577 |
| CDS Mutation | c.1858C>T |
| AA Mutation | p.Arg620Cys(p.R620C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38566524:38566524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3725C>T |
| AA Mutation | p.Ala1242Val(p.A1242V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38579483:38579483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3241C>G |
| AA Mutation | p.Pro1081Ala(p.P1081A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38551459:38551459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374557801 |
| CDS Mutation | c.4913G>A |
| AA Mutation | p.Arg1638Gln(p.R1638Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38551550:38551550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4822C>A |
| AA Mutation | p.Leu1608Ile(p.L1608I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38554528:38554528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4564T>A |
| AA Mutation | p.Phe1522Ile(p.F1522I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38608191:38608191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.958A>G |
| AA Mutation | p.Thr320Ala(p.T320A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38560241:38560241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4151G>A |
| AA Mutation | p.Cys1384Tyr(p.C1384Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38550671:38550671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473325 |
| CDS Mutation | c.5701G>A |
| AA Mutation | p.Glu1901Lys(p.E1901K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38550947:38550947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5425A>G |
| AA Mutation | p.Ile1809Val(p.I1809V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38606773:38606773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368552426 |
| CDS Mutation | c.1036G>A |
| AA Mutation | p.Glu346Lys(p.E346K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38606136:38606136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771588294 |
| CDS Mutation | c.1153G>A |
| AA Mutation | p.Ala385Thr(p.A385T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38599036:38599036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1905G>T |
| AA Mutation | p.Glu635Asp(p.E635D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38551240:38551240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5132C>T |
| AA Mutation | p.Ala1711Val(p.A1711V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38551453:38551453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4919C>G |
| AA Mutation | p.Ala1640Gly(p.A1640G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38613773:38613773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473072 |
| CDS Mutation | c.673C>T |
| AA Mutation | p.Arg225Trp(p.R225W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38551469:38551469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4903A>G |
| AA Mutation | p.Arg1635Gly(p.R1635G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38560374:38560374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473605 |
| CDS Mutation | c.4018G>A |
| AA Mutation | p.Val1340Ile(p.V1340I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38550937:38550937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371891414 |
| CDS Mutation | c.5435C>T |
| AA Mutation | p.Ser1812Leu(p.S1812L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38550371:38550371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6001C>T |
| AA Mutation | p.Leu2001Phe(p.L2001F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38560398:38560398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs794728877 |
| CDS Mutation | c.3994C>T |
| AA Mutation | p.Pro1332Ser(p.P1332S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38609866:38609866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750990576 |
| CDS Mutation | c.802G>A |
| AA Mutation | p.Gly268Ser(p.G268S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38599017:38599017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1924A>C |
| AA Mutation | p.Met642Leu(p.M642L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38575380:38575380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3583C>T |
| AA Mutation | p.Arg1195Cys(p.R1195C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38562470:38562470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3908G>A |
| AA Mutation | p.Arg1303Gln(p.R1303Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38551403:38551403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4969C>A |
| AA Mutation | p.Leu1657Ile(p.L1657I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38630317:38630317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.386T>C |
| AA Mutation | p.Val129Ala(p.V129A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38609777:38609777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529144420 |
| CDS Mutation | c.891C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38581345:38581345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2814G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38608156:38608156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757715398 |
| CDS Mutation | c.993C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38554373:38554373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754221948 |
| CDS Mutation | c.4719C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38560405:38560405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761384669 |
| CDS Mutation | c.3987C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38597738:38597738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371649934 |
| CDS Mutation | c.2253C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38587484:38587484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2352C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38555692:38555692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4506C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38575360:38575360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775488050 |
| CDS Mutation | c.3603C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38551005:38551005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375752426 |
| CDS Mutation | c.5367C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38598928:38598928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751050999 |
| CDS Mutation | c.2013C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38606795:38606795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1014C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38609780:38609780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774132896 |
| CDS Mutation | c.888C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38576689:38576689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3483C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38551305:38551305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557836660 |
| CDS Mutation | c.5067C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38550366:38550366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749546972 |
| CDS Mutation | c.6006C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000333535 |
| Start | 38604771:38604771(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1476delC |
| AA Mutation | p.Asp492GlufsTer15(p.D492Efs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000333535 |
| Start | 38551460:38551460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761505217 |
| CDS Mutation | c.4912C>T |
| AA Mutation | p.Arg1638Ter(p.R1638*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |