Primary Site >> Stomach Cancer
Gene >> NRXN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50538549:50538549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1847G>T |
| AA Mutation | p.Gly616Val(p.G616V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51028020:51028020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200849814 |
| CDS Mutation | c.254G>A |
| AA Mutation | p.Arg85His(p.R85H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50552794:50552794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569617213 |
| CDS Mutation | c.1552T>G |
| AA Mutation | p.Leu518Val(p.L518V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50497553:50497553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs796052780 |
| CDS Mutation | c.2659G>A |
| AA Mutation | p.Asp887Asn(p.D887N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50497676:50497676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2536A>T |
| AA Mutation | p.Asn846Tyr(p.N846Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 49943763:49943763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4067C>T |
| AA Mutation | p.Ala1356Val(p.A1356V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51028224:51028224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.50C>T |
| AA Mutation | p.Ser17Leu(p.S17L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027871:51027871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.403G>A |
| AA Mutation | p.Ala135Thr(p.A135T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 49943713:49943713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4117G>T |
| AA Mutation | p.Gly1373Cys(p.G1373C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027831:51027831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.443C>T |
| AA Mutation | p.Thr148Met(p.T148M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50053530:50053530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3779G>A |
| AA Mutation | p.Gly1260Asp(p.G1260D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000406316 |
| Start | 50053588:50053588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3721C>T |
| AA Mutation | p.Arg1241Cys(p.R1241C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50053543:50053543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3766G>A |
| AA Mutation | p.Gly1256Arg(p.G1256R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50552876:50552876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1470C>A |
| AA Mutation | p.Phe490Leu(p.F490L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50091331:50091331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3710A>G |
| AA Mutation | p.Tyr1237Cys(p.Y1237C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50552729:50552729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1617C>A |
| AA Mutation | p.Asp539Glu(p.D539E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50623550:50623550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.898C>T |
| AA Mutation | p.Pro300Ser(p.P300S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51028012:51028012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.262C>T |
| AA Mutation | p.Arg88Cys(p.R88C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51028081:51028081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.193G>A |
| AA Mutation | p.Gly65Ser(p.G65S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027867:51027867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.407A>C |
| AA Mutation | p.Lys136Thr(p.K136T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50053462:50053462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756844822 |
| CDS Mutation | c.3847G>A |
| AA Mutation | p.Glu1283Lys(p.E1283K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 49922120:49922120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4258T>C |
| AA Mutation | p.Tyr1420His(p.Y1420H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50497438:50497438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2774C>A |
| AA Mutation | p.Thr925Asn(p.T925N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50553019:50553019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1327T>A |
| AA Mutation | p.Tyr443Asn(p.Y443N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50236845:50236845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201881725 |
| CDS Mutation | c.3490G>A |
| AA Mutation | p.Val1164Ile(p.V1164I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50623444:50623444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1004T>C |
| AA Mutation | p.Leu335Pro(p.L335P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50053374:50053374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201323039 |
| CDS Mutation | c.3935C>T |
| AA Mutation | p.Ala1312Val(p.A1312V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 49922131:49922131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4247T>G |
| AA Mutation | p.Leu1416Arg(p.L1416R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50552649:50552649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1697T>C |
| AA Mutation | p.Leu566Pro(p.L566P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51028093:51028093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.181C>T |
| AA Mutation | p.Arg61Cys(p.R61C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50053410:50053410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3899T>C |
| AA Mutation | p.Val1300Ala(p.V1300A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50091335:50091335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3706C>T |
| AA Mutation | p.Arg1236Cys(p.R1236C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50091334:50091334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200658010 |
| CDS Mutation | c.3707G>A |
| AA Mutation | p.Arg1236His(p.R1236H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027904:51027904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202244228 |
| CDS Mutation | c.370C>T |
| AA Mutation | p.Arg124Cys(p.R124C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51028045:51028045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.229G>A |
| AA Mutation | p.Asp77Asn(p.D77N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50538426:50538426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781319797 |
| CDS Mutation | c.1970G>A |
| AA Mutation | p.Arg657Gln(p.R657Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 50053419:50053419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3890T>G |
| AA Mutation | p.Val1297Gly(p.V1297G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027862:51027862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374644929 |
| CDS Mutation | c.412G>T |
| AA Mutation | p.Val138Leu(p.V138L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027819:51027819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.455G>A |
| AA Mutation | p.Gly152Asp(p.G152D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027651:51027651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748372282 |
| CDS Mutation | c.623C>T |
| AA Mutation | p.Pro208Leu(p.P208L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 49922131:49922131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4247T>C |
| AA Mutation | p.Leu1416Pro(p.L1416P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000406316 |
| Start | 51028149:51028149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.125G>A |
| AA Mutation | p.Arg42His(p.R42H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50236879:50236879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3456G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 49943720:49943720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762505334 |
| CDS Mutation | c.4110G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027521:51027521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770481343 |
| CDS Mutation | c.753C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50506580:50506580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2412C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027947:51027947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.327T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027827:51027827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.447G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50091471:50091471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3570G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 51028019:51028019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.255C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50623608:50623608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.840A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50236954:50236954(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3381C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50623419:50623419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1029C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50053586:50053586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3723T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 51028046:51028046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765374506 |
| CDS Mutation | c.228C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027794:51027794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771181102 |
| CDS Mutation | c.480G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50553020:50553020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1326A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 51028013:51028013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587781102 |
| CDS Mutation | c.261C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027605:51027605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.669C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 49921998:49921998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4380T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027785:51027785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747224688 |
| CDS Mutation | c.489C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50497653:50497653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2559A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50497644:50497644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372107588 |
| CDS Mutation | c.2568G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50552786:50552786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1560C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 51027536:51027536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201209196 |
| CDS Mutation | c.738G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000406316 |
| Start | 50506571:50506571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115211871 |
| CDS Mutation | c.2421C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |