ClinVar Miner

List of variants in gene SRPX2 studied for epilepsy

Included ClinVar conditions (435):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 92
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014467.3(SRPX2):c.356-38G>A rs2022475 0.83087
NM_014467.3(SRPX2):c.163+12T>C rs73555462 0.02331
NM_014467.3(SRPX2):c.460C>G (p.His154Asp) rs73636611 0.00298
NM_014467.3(SRPX2):c.1030C>A (p.Leu344Ile) rs149051060 0.00145
NM_014467.3(SRPX2):c.1373G>A (p.Arg458Gln) rs146051561 0.00133
NM_014467.3(SRPX2):c.840G>A (p.Ala280=) rs139377205 0.00118
NM_014467.3(SRPX2):c.481C>A (p.Arg161=) rs150552508 0.00101
NM_014467.3(SRPX2):c.918T>C (p.Cys306=) rs34728871 0.00080
NM_014467.3(SRPX2):c.1293C>T (p.Tyr431=) rs138091242 0.00050
NM_014467.3(SRPX2):c.980A>G (p.Asn327Ser) rs121918363 0.00041
NM_014467.3(SRPX2):c.809C>T (p.Pro270Leu) rs148735447 0.00030
NM_014467.3(SRPX2):c.737G>A (p.Arg246Gln) rs146063801 0.00026
NM_014467.3(SRPX2):c.323G>A (p.Ser108Asn) rs200483534 0.00023
NM_014467.3(SRPX2):c.693C>A (p.His231Gln) rs142719253 0.00022
NM_014467.3(SRPX2):c.1218-6C>T rs370981134 0.00019
NM_014467.3(SRPX2):c.449C>T (p.Ser150Phe) rs373847965 0.00019
NM_014467.3(SRPX2):c.624G>A (p.Pro208=) rs139514583 0.00018
NM_014467.3(SRPX2):c.1221A>G (p.Gln407=) rs375935170 0.00017
NM_014467.3(SRPX2):c.920A>G (p.Gln307Arg) rs147757229 0.00017
NM_014467.3(SRPX2):c.564C>T (p.His188=) rs149317696 0.00015
NM_014467.3(SRPX2):c.1199A>G (p.Asn400Ser) rs141292909 0.00011
NM_014467.3(SRPX2):c.893G>A (p.Arg298His) rs369663551 0.00011
NM_014467.3(SRPX2):c.257G>A (p.Arg86His) rs776691028 0.00010
NM_014467.3(SRPX2):c.981C>G (p.Asn327Lys) rs370033099 0.00009
NM_014467.3(SRPX2):c.248T>C (p.Leu83Pro) rs141168255 0.00007
NM_014467.3(SRPX2):c.160C>A (p.Arg54=) rs772122754 0.00005
NM_014467.3(SRPX2):c.221C>T (p.Pro74Leu) rs773892997 0.00005
NM_014467.3(SRPX2):c.224A>T (p.Lys75Met) rs767072861 0.00005
NM_014467.3(SRPX2):c.882C>T (p.Gly294=) rs748732647 0.00005
NM_014467.3(SRPX2):c.1144G>A (p.Val382Met) rs148241932 0.00004
NM_014467.3(SRPX2):c.369C>T (p.His123=) rs370296491 0.00004
NM_014467.3(SRPX2):c.1011A>G (p.Gln337=) rs146920180 0.00003
NM_014467.3(SRPX2):c.1288C>T (p.Arg430Cys) rs757158053 0.00003
NM_014467.3(SRPX2):c.215A>C (p.Tyr72Ser) rs121918364 0.00003
NM_014467.3(SRPX2):c.305C>T (p.Ser102Leu) rs1237471672 0.00003
NM_014467.3(SRPX2):c.959C>T (p.Ala320Val) rs780126596 0.00003
NM_014467.3(SRPX2):c.982G>A (p.Val328Ile) rs753573260 0.00003
NM_014467.3(SRPX2):c.99G>A (p.Pro33=) rs766670891 0.00003
NM_014467.3(SRPX2):c.1229G>A (p.Arg410His) rs368571175 0.00002
NM_014467.3(SRPX2):c.1276A>G (p.Ile426Val) rs756623285 0.00002
NM_014467.3(SRPX2):c.1289G>A (p.Arg430His) rs183378773 0.00002
NM_014467.3(SRPX2):c.329G>A (p.Arg110His) rs1176341753 0.00002
NM_014467.3(SRPX2):c.553C>T (p.Arg185Cys) rs370080258 0.00002
NM_014467.3(SRPX2):c.554G>T (p.Arg185Leu) rs768629864 0.00002
NM_014467.3(SRPX2):c.648T>C (p.Gly216=) rs751951110 0.00002
NM_014467.3(SRPX2):c.961+1G>A rs1303998333 0.00002
NM_014467.3(SRPX2):c.1028G>A (p.Arg343Gln) rs1060502322 0.00001
NM_014467.3(SRPX2):c.1133T>C (p.Ile378Thr) rs1483904597 0.00001
NM_014467.3(SRPX2):c.1238G>A (p.Arg413His) rs761966457 0.00001
NM_014467.3(SRPX2):c.1255G>A (p.Val419Met) rs797046012 0.00001
NM_014467.3(SRPX2):c.161G>A (p.Arg54Gln) rs761225832 0.00001
NM_014467.3(SRPX2):c.174G>C (p.Trp58Cys) rs1354537844 0.00001
NM_014467.3(SRPX2):c.202G>A (p.Glu68Lys) rs747055996 0.00001
NM_014467.3(SRPX2):c.370G>A (p.Ala124Thr) rs746716311 0.00001
NM_014467.3(SRPX2):c.371C>T (p.Ala124Val) rs1277274875 0.00001
NM_014467.3(SRPX2):c.431G>A (p.Arg144His) rs758942073 0.00001
NM_014467.3(SRPX2):c.57G>A (p.Pro19=) rs192241917 0.00001
NM_014467.3(SRPX2):c.646G>A (p.Gly216Ser) rs758845090 0.00001
NM_014467.3(SRPX2):c.742T>C (p.Tyr248His) rs1208754092 0.00001
NC_000023.11:g.(?_100646303)_(100671007_?)dup
NM_014467.3(SRPX2):c.1046C>G (p.Ala349Gly) rs2083208096
NM_014467.3(SRPX2):c.1129A>G (p.Thr377Ala) rs1355036934
NM_014467.3(SRPX2):c.112_163+10dup rs2083150642
NM_014467.3(SRPX2):c.1143G>A (p.Leu381=) rs2083214837
NM_014467.3(SRPX2):c.117A>C (p.Glu39Asp) rs762469858
NM_014467.3(SRPX2):c.1183C>T (p.Gln395Ter) rs771849296
NM_014467.3(SRPX2):c.118G>A (p.Val40Ile)
NM_014467.3(SRPX2):c.1311C>T (p.Pro437=) rs2083222587
NM_014467.3(SRPX2):c.1313A>T (p.Glu438Val) rs1047926579
NM_014467.3(SRPX2):c.1365C>T (p.Thr455=) rs1602727943
NM_014467.3(SRPX2):c.1396T>G (p.Ter466Gly)
NM_014467.3(SRPX2):c.17C>T (p.Thr6Ile) rs1556010625
NM_014467.3(SRPX2):c.207C>T (p.Ala69=)
NM_014467.3(SRPX2):c.355+8G>T rs772952088
NM_014467.3(SRPX2):c.366C>T (p.Cys122=) rs2147648869
NM_014467.3(SRPX2):c.466G>C (p.Glu156Gln)
NM_014467.3(SRPX2):c.49C>G (p.Leu17Val) rs1422524189
NM_014467.3(SRPX2):c.560C>T (p.Pro187Leu) rs1569361725
NM_014467.3(SRPX2):c.586C>A (p.Pro196Thr) rs1398023125
NM_014467.3(SRPX2):c.602C>T (p.Ala201Val) rs915881767
NM_014467.3(SRPX2):c.605G>A (p.Arg202Gln) rs200784551
NM_014467.3(SRPX2):c.656C>G (p.Thr219Ser) rs924461236
NM_014467.3(SRPX2):c.659+8_659+22del rs1378393239
NM_014467.3(SRPX2):c.659G>C (p.Arg220Thr)
NM_014467.3(SRPX2):c.706G>C (p.Glu236Gln) rs754500495
NM_014467.3(SRPX2):c.723C>T (p.Tyr241=)
NM_014467.3(SRPX2):c.725C>G (p.Thr242Ser) rs2083202209
NM_014467.3(SRPX2):c.732T>C (p.Tyr244=) rs1556013511
NM_014467.3(SRPX2):c.928C>T (p.Arg310Cys) rs758448998
NM_014467.3(SRPX2):c.975C>T (p.Asn325=) rs2083207723
NM_014467.3(SRPX2):c.981C>T (p.Asn327=) rs370033099
NM_014467.3(SRPX2):c.99G>T (p.Pro33=) rs766670891

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.