ClinVar Miner

List of variants in gene DSE studied for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 121
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_013352.4(DSE):c.*287A>G rs472762 0.82042
NM_013352.4(DSE):c.-53-232T>A rs1557547 0.70872
NM_013352.4(DSE):c.911-50G>T rs574278 0.66786
NM_001080976.3(DSE):c.-54+134A>G rs6909152 0.45462
NM_001080976.3(DSE):c.-54+109A>G rs6909133 0.40670
NM_013352.4(DSE):c.1119-83G>A rs479454 0.34969
NM_001080976.3(DSE):c.-192G>C rs9400898 0.23999
NM_001080976.3(DSE):c.-54+184A>T rs62423798 0.19357
NM_013352.4(DSE):c.911-229G>A rs3213531 0.05459
NM_013352.4(DSE):c.*149C>T rs471134 0.04839
NM_013352.4(DSE):c.1118+43G>A rs9942469 0.01609
NM_013352.4(DSE):c.671-211A>G rs143281839 0.01457
NM_013352.4(DSE):c.-53-89A>G rs115024541 0.01409
NM_013352.4(DSE):c.*228T>G rs115358868 0.01375
NM_013352.4(DSE):c.1119-285C>G rs17256693 0.01198
NM_013352.4(DSE):c.671-286A>G rs112076286 0.01198
NM_013352.4(DSE):c.911-231A>C rs192288523 0.00570
NM_013352.4(DSE):c.114C>T (p.Ala38=) rs36061922 0.00553
NM_013352.4(DSE):c.416+296A>G rs112653287 0.00543
NM_013352.4(DSE):c.711G>C (p.Leu237=) rs140034597 0.00464
NM_013352.4(DSE):c.417-50A>G rs113394683 0.00397
NM_013352.4(DSE):c.911-114C>T rs553641167 0.00197
NM_013352.4(DSE):c.911-251G>A rs184434279 0.00183
NM_013352.4(DSE):c.2651G>A (p.Arg884Gln) rs35363262 0.00180
NM_013352.4(DSE):c.2120C>G (p.Ser707Cys) rs140975523 0.00153
NM_013352.4(DSE):c.216G>A (p.Thr72=) rs61747210 0.00150
NM_013352.4(DSE):c.1961G>A (p.Arg654Gln) rs61741781 0.00109
NM_013352.4(DSE):c.2687T>G (p.Leu896Arg) rs149649831 0.00052
NM_013352.4(DSE):c.1173G>A (p.Leu391=) rs146663575 0.00050
NM_013352.4(DSE):c.1653G>A (p.Leu551=) rs147124340 0.00050
NM_013352.4(DSE):c.1004G>A (p.Arg335His) rs371480627 0.00029
NM_013352.4(DSE):c.35T>A (p.Phe12Tyr) rs142885560 0.00024
NM_013352.4(DSE):c.2761A>G (p.Thr921Ala) rs143226402 0.00021
NM_013352.4(DSE):c.450G>A (p.Pro150=) rs773416085 0.00018
NM_013352.4(DSE):c.1221T>A (p.Pro407=) rs140103226 0.00015
NM_013352.4(DSE):c.2727T>C (p.Ile909=) rs199742443 0.00015
NM_013352.4(DSE):c.240C>T (p.Ser80=) rs143347973 0.00014
NM_013352.4(DSE):c.2083G>A (p.Ala695Thr) rs148394823 0.00013
NM_013352.4(DSE):c.1383T>A (p.Ala461=) rs200485959 0.00011
NM_013352.4(DSE):c.2005A>G (p.Ile669Val) rs145999978 0.00011
NM_013352.4(DSE):c.2168G>A (p.Arg723Gln) rs371043332 0.00011
NM_013352.4(DSE):c.2842T>C (p.Trp948Arg) rs146336077 0.00011
NM_013352.4(DSE):c.645G>A (p.Thr215=) rs370613241 0.00011
NM_013352.4(DSE):c.68A>G (p.Tyr23Cys) rs140339574 0.00011
NM_013352.4(DSE):c.359T>C (p.Ile120Thr) rs147451395 0.00010
NM_013352.4(DSE):c.1860C>T (p.Asp620=) rs376227527 0.00007
NM_013352.4(DSE):c.208C>T (p.Arg70Cys) rs375337613 0.00006
NM_013352.4(DSE):c.826G>A (p.Val276Ile) rs754514077 0.00006
NM_013352.4(DSE):c.-53-4G>A rs763584486 0.00005
NM_013352.4(DSE):c.2016G>A (p.Gln672=) rs772695668 0.00005
NM_013352.4(DSE):c.2429G>A (p.Arg810Gln) rs367959320 0.00005
NM_013352.4(DSE):c.2508T>G (p.Ile836Met) rs147927564 0.00005
NM_013352.4(DSE):c.936G>A (p.Ala312=) rs543521325 0.00005
NM_013352.4(DSE):c.2082C>T (p.Tyr694=) rs776273558 0.00004
NM_013352.4(DSE):c.215C>T (p.Thr72Met) rs201564300 0.00004
NM_013352.4(DSE):c.95T>C (p.Met32Thr) rs140765634 0.00004
NM_013352.4(DSE):c.1841A>G (p.Tyr614Cys) rs749683894 0.00003
NM_013352.4(DSE):c.1913G>A (p.Gly638Asp) rs372851752 0.00003
NM_013352.4(DSE):c.2147G>A (p.Arg716His) rs549153887 0.00003
NM_013352.4(DSE):c.670+12C>T rs190922886 0.00003
NM_013352.4(DSE):c.1582G>A (p.Ala528Thr) rs773958566 0.00002
NM_013352.4(DSE):c.1927G>A (p.Gly643Arg) rs758269032 0.00002
NM_013352.4(DSE):c.193G>A (p.Glu65Lys) rs772898380 0.00002
NM_013352.4(DSE):c.2370T>C (p.Ile790=) rs145906435 0.00002
NM_013352.4(DSE):c.2428C>G (p.Arg810Gly) rs199731077 0.00002
NM_013352.4(DSE):c.693A>G (p.Leu231=) rs747871581 0.00002
NM_013352.4(DSE):c.780G>A (p.Ala260=) rs765697282 0.00002
NM_013352.4(DSE):c.1437C>T (p.Phe479=) rs757356537 0.00001
NM_013352.4(DSE):c.144C>T (p.Phe48=) rs562789659 0.00001
NM_013352.4(DSE):c.1512A>G (p.Glu504=) rs200018749 0.00001
NM_013352.4(DSE):c.1609A>T (p.Ile537Phe) rs1213902929 0.00001
NM_013352.4(DSE):c.1613G>A (p.Arg538Gln) rs776857406 0.00001
NM_013352.4(DSE):c.17G>A (p.Arg6Gln) rs758271302 0.00001
NM_013352.4(DSE):c.1875C>T (p.Ser625=) rs771082377 0.00001
NM_013352.4(DSE):c.1909C>T (p.Arg637Trp) rs763787753 0.00001
NM_013352.4(DSE):c.2075A>G (p.His692Arg) rs374283523 0.00001
NM_013352.4(DSE):c.2186G>A (p.Ser729Asn) rs779169990 0.00001
NM_013352.4(DSE):c.2192T>C (p.Ile731Thr) rs746129064 0.00001
NM_013352.4(DSE):c.2334G>T (p.Leu778=) rs534248134 0.00001
NM_013352.4(DSE):c.2389T>C (p.Ser797Pro) rs1784193105 0.00001
NM_013352.4(DSE):c.2510G>A (p.Arg837Lys) rs1213224276 0.00001
NM_013352.4(DSE):c.2608C>T (p.His870Tyr) rs746254694 0.00001
NM_013352.4(DSE):c.285T>G (p.Ser95Arg) rs781449748 0.00001
NM_013352.4(DSE):c.495G>T (p.Leu165Phe) rs1057524129 0.00001
NM_013352.4(DSE):c.557G>T (p.Gly186Val) rs1025167723 0.00001
NM_013352.4(DSE):c.75C>T (p.Thr25=) rs752936676 0.00001
NM_013352.4(DSE):c.891G>A (p.Met297Ile) rs768909519 0.00001
NM_013352.4(DSE):c.1000A>G (p.Met334Val)
NM_013352.4(DSE):c.110A>T (p.Asn37Ile) rs371802983
NM_013352.4(DSE):c.1169C>T (p.Thr390Ile)
NM_013352.4(DSE):c.1284T>C (p.Tyr428=) rs1583235798
NM_013352.4(DSE):c.1334A>G (p.Asn445Ser) rs1423707879
NM_013352.4(DSE):c.1420G>A (p.Gly474Arg) rs1245898059
NM_013352.4(DSE):c.1428G>A (p.Lys476=) rs1554228114
NM_013352.4(DSE):c.1522T>A (p.Ser508Thr)
NM_013352.4(DSE):c.161C>T (p.Ala54Val)
NM_013352.4(DSE):c.1752G>C (p.Ala584=) rs561665809
NM_013352.4(DSE):c.1819A>T (p.Ile607Phe)
NM_013352.4(DSE):c.1897G>A (p.Val633Met) rs550208733
NM_013352.4(DSE):c.2058C>T (p.Phe686=) rs1562314835
NM_013352.4(DSE):c.2091C>G (p.Tyr697Ter) rs2482304968
NM_013352.4(DSE):c.2298C>T (p.Asn766=) rs1583238314
NM_013352.4(DSE):c.22dup (p.Ala8fs) rs2482082556
NM_013352.4(DSE):c.2387T>C (p.Ile796Thr) rs2482307341
NM_013352.4(DSE):c.2428C>T (p.Arg810Ter) rs199731077
NM_013352.4(DSE):c.2511A>T (p.Arg837Ser) rs2482308242
NM_013352.4(DSE):c.2619_2621del (p.Gly874del) rs111252008
NM_013352.4(DSE):c.2620G>A (p.Gly874Ser)
NM_013352.4(DSE):c.2635C>G (p.Arg879Gly) rs113277624
NM_013352.4(DSE):c.2635C>T (p.Arg879Trp) rs113277624
NM_013352.4(DSE):c.29G>A (p.Ser10Asn) rs749737486
NM_013352.4(DSE):c.330A>C (p.Ala110=) rs1583172878
NM_013352.4(DSE):c.416+1G>A rs2482086431
NM_013352.4(DSE):c.417-15T>G rs377249948
NM_013352.4(DSE):c.495G>A (p.Leu165=) rs1057524129
NM_013352.4(DSE):c.558G>T (p.Gly186=) rs1583220200
NM_013352.4(DSE):c.670+328del rs34766242
NM_013352.4(DSE):c.671-165dup rs11389417
NM_013352.4(DSE):c.796A>G (p.Thr266Ala) rs1283836708
NM_013352.4(DSE):c.831G>A (p.Gln277=) rs1583228126
NM_013352.4(DSE):c.881T>G (p.Phe294Cys)

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.