Primary Site >> Stomach Cancer
Gene >> PREX2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68055852:68055852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1116A>C |
| AA Mutation | p.Gln372His(p.Q372H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68115872:68115872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763886172 |
| CDS Mutation | c.3266T>C |
| AA Mutation | p.Val1089Ala(p.V1089A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68134265:68134265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3973T>C |
| AA Mutation | p.Ser1325Pro(p.S1325P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68099779:68099779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2651A>C |
| AA Mutation | p.Lys884Thr(p.K884T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000288368 |
| Start | 68019670:68019670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.335T>C |
| AA Mutation | p.Phe112Ser(p.F112S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68099764:68099764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2636C>A |
| AA Mutation | p.Thr879Asn(p.T879N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68044501:68044501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.854G>A |
| AA Mutation | p.Ser285Asn(p.S285N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68099725:68099725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2597A>C |
| AA Mutation | p.Asn866Thr(p.N866T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68083324:68083324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1963T>G |
| AA Mutation | p.Phe655Val(p.F655V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68027243:68027243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139157434 |
| CDS Mutation | c.463C>T |
| AA Mutation | p.Arg155Trp(p.R155W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68080786:68080786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1826A>G |
| AA Mutation | p.Asp609Gly(p.D609G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68053199:68053199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1046A>T |
| AA Mutation | p.Lys349Met(p.K349M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68077425:68077425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1598T>A |
| AA Mutation | p.Met533Lys(p.M533K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68080457:68080457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs529924687 |
| CDS Mutation | c.1657G>A |
| AA Mutation | p.Glu553Lys(p.E553K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68224585:68224585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4734G>T |
| AA Mutation | p.Lys1578Asn(p.K1578N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68121010:68121010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs530869739 |
| CDS Mutation | c.3685G>A |
| AA Mutation | p.Val1229Ile(p.V1229I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000288368 |
| Start | 68192525:68192525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754115767 |
| CDS Mutation | c.4604G>A |
| AA Mutation | p.Arg1535Gln(p.R1535Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68053153:68053153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1000G>A |
| AA Mutation | p.Ala334Thr(p.A334T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68099761:68099761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2633C>A |
| AA Mutation | p.Pro878His(p.P878H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68077407:68077407(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767992923 |
| CDS Mutation | c.1580G>A |
| AA Mutation | p.Arg527His(p.R527H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68099828:68099828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2700A>G |
| AA Mutation | p.Ile900Met(p.I900M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68019664:68019664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.329T>C |
| AA Mutation | p.Leu110Pro(p.L110P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68119472:68119472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3462A>T |
| AA Mutation | p.Lys1154Asn(p.K1154N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68038241:68038241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.788G>A |
| AA Mutation | p.Arg263Gln(p.R263Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68097112:68097112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs190776975 |
| CDS Mutation | c.2464G>A |
| AA Mutation | p.Val822Met(p.V822M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68017852:68017852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.148T>A |
| AA Mutation | p.Leu50Ile(p.L50I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68090603:68090603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2138T>G |
| AA Mutation | p.Leu713Arg(p.L713R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68069064:68069064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1371G>T |
| AA Mutation | p.Gln457His(p.Q457H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68224581:68224581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200020354 |
| CDS Mutation | c.4730C>T |
| AA Mutation | p.Ala1577Val(p.A1577V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68097056:68097056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2408G>A |
| AA Mutation | p.Gly803Glu(p.G803E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68157424:68157424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4334A>C |
| AA Mutation | p.Asn1445Thr(p.N1445T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68017852:68017852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.148T>G |
| AA Mutation | p.Leu50Val(p.L50V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68090582:68090582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2117C>G |
| AA Mutation | p.Thr706Ser(p.T706S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68030518:68030518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770289181 |
| CDS Mutation | c.565C>T |
| AA Mutation | p.Arg189Trp(p.R189W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68017897:68017897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.193G>T |
| AA Mutation | p.Val65Leu(p.V65L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68017898:68017898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.194T>A |
| AA Mutation | p.Val65Glu(p.V65E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68069851:68069851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1460G>T |
| AA Mutation | p.Cys487Phe(p.C487F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000288368 |
| Start | 68120196:68120196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3505G>T |
| AA Mutation | p.Val1169Leu(p.V1169L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68119480:68119480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3470A>C |
| AA Mutation | p.Lys1157Thr(p.K1157T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000288368 |
| Start | 68134274:68134274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557338072 |
| CDS Mutation | c.3982T>G |
| AA Mutation | p.Leu1328Val(p.L1328V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68030512:68030512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.559A>G |
| AA Mutation | p.Thr187Ala(p.T187A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68087753:68087753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2057G>A |
| AA Mutation | p.Gly686Glu(p.G686E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68017907:68017907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774177545 |
| CDS Mutation | c.203A>G |
| AA Mutation | p.Glu68Gly(p.E68G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68080496:68080496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1696G>A |
| AA Mutation | p.Asp566Asn(p.D566N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68099782:68099782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2654T>G |
| AA Mutation | p.Phe885Cys(p.F885C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68146234:68146234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4113A>C |
| AA Mutation | p.Glu1371Asp(p.E1371D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68192413:68192413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4492T>C |
| AA Mutation | p.Cys1498Arg(p.C1498R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68134106:68134106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3814G>T |
| AA Mutation | p.Val1272Leu(p.V1272L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68134190:68134190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3898A>C |
| AA Mutation | p.Thr1300Pro(p.T1300P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 67952513:67952513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.119G>A |
| AA Mutation | p.Gly40Asp(p.G40D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68060764:68060764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1324G>A |
| AA Mutation | p.Gly442Arg(p.G442R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288368 |
| Start | 68109466:68109466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758027463 |
| CDS Mutation | c.2989G>A |
| AA Mutation | p.Ala997Thr(p.A997T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68138453:68138453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4023A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68090670:68090670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2205C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68121033:68121033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766005867 |
| CDS Mutation | c.3708C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68115897:68115897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3291T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68146243:68146243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4122G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68217653:68217653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4642C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68157377:68157377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4287T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68192352:68192352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137974526 |
| CDS Mutation | c.4431C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 61 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 67952424:67952424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.30C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 62 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68109612:68109612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3135T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 63 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68044553:68044553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772618501 |
| CDS Mutation | c.906G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 64 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68093703:68093703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2349T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 65 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68083293:68083293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1932T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 66 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288368 |
| Start | 68108324:68108324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570753617 |
| CDS Mutation | c.2931G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |