ClinVar Miner

List of variants in gene UNG reported as likely benign for Hyper-IgM syndrome type 5

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 105
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HGVS dbSNP gnomAD frequency
NM_080911.3(UNG):c.*708T>C rs150677845 0.00341
NM_080911.3(UNG):c.*463C>T rs55947010 0.00170
NM_080911.3(UNG):c.533+6G>A rs55812333 0.00163
NM_080911.3(UNG):c.246G>C (p.Leu82=) rs144083363 0.00140
NM_080911.3(UNG):c.262C>T (p.Arg88Cys) rs151095402 0.00090
NM_080911.3(UNG):c.392C>T (p.Pro131Leu) rs140829672 0.00072
NM_080911.3(UNG):c.194C>T (p.Pro65Leu) rs199956941 0.00051
NM_080911.3(UNG):c.146A>G (p.Lys49Arg) rs143103316 0.00042
NM_080911.3(UNG):c.183G>A (p.Pro61=) rs147490205 0.00038
NM_080911.3(UNG):c.622+10C>T rs201555956 0.00026
NM_080911.3(UNG):c.522G>A (p.Pro174=) rs148037258 0.00017
NM_080911.3(UNG):c.339+15G>A rs368013839 0.00008
NM_080911.3(UNG):c.340-20C>T rs202212890 0.00007
NM_080911.3(UNG):c.622+9G>T rs774306202 0.00007
NM_080911.3(UNG):c.651G>A (p.Thr217=) rs141783420 0.00006
NM_080911.3(UNG):c.906G>A (p.Lys302=) rs561414480 0.00005
NM_080911.3(UNG):c.339+11A>C rs373929934 0.00004
NM_080911.3(UNG):c.623-10_623-9del rs1183424751 0.00004
NM_080911.3(UNG):c.738G>A (p.Ser246=) rs187858476 0.00004
NM_080911.3(UNG):c.81C>A (p.Ala27=) rs761928219 0.00004
NM_080911.3(UNG):c.312G>C (p.Gly104=) rs370788222 0.00003
NM_080911.3(UNG):c.36C>A (p.Ser12=) rs772832695 0.00003
NM_080911.3(UNG):c.486T>C (p.Ala162=) rs146685524 0.00003
NM_080911.3(UNG):c.771T>C (p.Tyr257=) rs1054086515 0.00003
NM_080911.3(UNG):c.802-20T>G rs1055056117 0.00003
NM_080911.3(UNG):c.895C>T (p.Leu299=) rs200129045 0.00003
NM_080911.3(UNG):c.90G>A (p.Gly30=) rs766467977 0.00003
NM_080911.3(UNG):c.186C>T (p.Pro62=) rs765545880 0.00002
NM_080911.3(UNG):c.285A>G (p.Gly95=) rs776852485 0.00002
NM_080911.3(UNG):c.801+14T>C rs770635458 0.00002
NM_080911.3(UNG):c.133-13_133-10dup rs751581970 0.00001
NM_080911.3(UNG):c.133-7C>T rs373087239 0.00001
NM_080911.3(UNG):c.141A>G (p.Pro47=) rs1455717438 0.00001
NM_080911.3(UNG):c.153C>G (p.Ala51=) rs1382771989 0.00001
NM_080911.3(UNG):c.267C>T (p.Asn89=) rs757301291 0.00001
NM_080911.3(UNG):c.303C>T (p.His101=) rs763266989 0.00001
NM_080911.3(UNG):c.339+18C>T rs749822150 0.00001
NM_080911.3(UNG):c.435+11C>T rs753987251 0.00001
NM_080911.3(UNG):c.435+9A>G rs764068836 0.00001
NM_080911.3(UNG):c.495C>T (p.Leu165=) rs2042181358 0.00001
NM_080911.3(UNG):c.513G>A (p.Arg171=) rs140301639 0.00001
NM_080911.3(UNG):c.533+15C>G rs752331296 0.00001
NM_080911.3(UNG):c.533+18G>A rs748871049 0.00001
NM_080911.3(UNG):c.534-14T>C rs1010413399 0.00001
NM_080911.3(UNG):c.622+11G>A rs775976001 0.00001
NM_080911.3(UNG):c.623-13C>G rs771114424 0.00001
NM_080911.3(UNG):c.633T>C (p.Leu211=) rs200572869 0.00001
NM_080911.3(UNG):c.639C>T (p.Asn213=) rs761526932 0.00001
NM_080911.3(UNG):c.825G>A (p.Thr275=) rs765151419 0.00001
NM_080911.3(UNG):c.843G>T (p.Leu281Phe) rs576935575 0.00001
NM_080911.3(UNG):c.133-19C>T rs749881834
NM_080911.3(UNG):c.133-8A>C rs757878186
NM_080911.3(UNG):c.135C>T (p.Ala45=) rs2499977711
NM_080911.3(UNG):c.138C>A (p.Ile46=) rs1479922084
NM_080911.3(UNG):c.150G>A (p.Lys50=)
NM_080911.3(UNG):c.159T>C (p.Ala53=)
NM_080911.3(UNG):c.168G>A (p.Glu56=) rs775726637
NM_080911.3(UNG):c.189C>G (p.Ser63=) rs2499977818
NM_080911.3(UNG):c.204C>G (p.Ala68=) rs777436497
NM_080911.3(UNG):c.237C>T (p.Ala79=) rs765568201
NM_080911.3(UNG):c.273C>G (p.Pro91=) rs758619136
NM_080911.3(UNG):c.273C>T (p.Pro91=) rs758619136
NM_080911.3(UNG):c.324A>G (p.Lys108=) rs2499978140
NM_080911.3(UNG):c.339+13A>G rs2499978184
NM_080911.3(UNG):c.36C>T (p.Ser12=) rs772832695
NM_080911.3(UNG):c.402C>T (p.Val134=)
NM_080911.3(UNG):c.408C>T (p.Thr136=) rs762887143
NM_080911.3(UNG):c.435+15T>A rs765672149
NM_080911.3(UNG):c.435+15T>C rs765672149
NM_080911.3(UNG):c.436-19G>A rs1395385244
NM_080911.3(UNG):c.471T>C (p.His157=) rs780271583
NM_080911.3(UNG):c.489C>T (p.His163=) rs376918741
NM_080911.3(UNG):c.519T>C (p.Val173=) rs1223036501
NM_080911.3(UNG):c.533+17G>T rs755840023
NM_080911.3(UNG):c.558G>A (p.Leu186=)
NM_080911.3(UNG):c.60C>T (p.His20=) rs770972381
NM_080911.3(UNG):c.622+16C>T rs2042189211
NM_080911.3(UNG):c.622+18dup
NM_080911.3(UNG):c.622+19G>C rs1055032550
NM_080911.3(UNG):c.622+20A>T rs963729277
NM_080911.3(UNG):c.623-11C>G rs1566121868
NM_080911.3(UNG):c.623-15C>A rs780850116
NM_080911.3(UNG):c.623-15C>T
NM_080911.3(UNG):c.623-9T>C rs745983593
NM_080911.3(UNG):c.654T>C (p.Val218=) rs759689813
NM_080911.3(UNG):c.681G>A (p.Lys227=) rs746124875
NM_080911.3(UNG):c.696G>A (p.Glu232=) rs2135887528
NM_080911.3(UNG):c.732G>A (p.Gln244=) rs193922715
NM_080911.3(UNG):c.738G>T (p.Ser246=) rs187858476
NM_080911.3(UNG):c.744C>G (p.Gly248=) rs1593322263
NM_080911.3(UNG):c.783G>A (p.Lys261=) rs1457717204
NM_080911.3(UNG):c.801+16T>C rs2499983515
NM_080911.3(UNG):c.801+18T>C rs773820400
NM_080911.3(UNG):c.801+19_801+21del
NM_080911.3(UNG):c.801+19_801+22del rs1347611424
NM_080911.3(UNG):c.802-12G>C rs745539300
NM_080911.3(UNG):c.802-15C>A rs2042247136
NM_080911.3(UNG):c.802-18A>G
NM_080911.3(UNG):c.802-9C>T rs2499990276
NM_080911.3(UNG):c.819A>G (p.Leu273=) rs1593326380
NM_080911.3(UNG):c.858G>A (p.Gly286=)
NM_080911.3(UNG):c.888C>G (p.Thr296=)
NM_080911.3(UNG):c.888C>T (p.Thr296=)
NM_080911.3(UNG):c.90G>T (p.Gly30=) rs766467977
NM_080911.3(UNG):c.924T>A (p.Ile308=) rs765063470

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