List of variants in gene UNG reported as likely benign for B cell deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 96

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HGVS	dbSNP	gnomAD frequency
NM_080911.3(UNG):c.*708T>C	rs150677845	0.00374
NM_080911.3(UNG):c.*463C>T	rs55947010	0.00178
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	0.00046
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.906G>A (p.Lys302=)	rs561414480	0.00010
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	0.00005
NM_080911.3(UNG):c.339+11A>C	rs373929934	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.36C>A (p.Ser12=)	rs772832695	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.186C>T (p.Pro62=)	rs765545880	0.00002
NM_080911.3(UNG):c.285A>G (p.Gly95=)	rs776852485	0.00002
NM_080911.3(UNG):c.486T>C (p.Ala162=)	rs146685524	0.00002
NM_080911.3(UNG):c.533+15C>G	rs752331296	0.00002
NM_080911.3(UNG):c.801+14T>C	rs770635458	0.00002
NM_080911.3(UNG):c.133-7C>T	rs373087239	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.513G>A (p.Arg171=)	rs140301639	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.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.681G>A (p.Lys227=)	rs746124875	0.00001
NM_080911.3(UNG):c.843G>T (p.Leu281Phe)	rs576935575	0.00001
NM_080911.3(UNG):c.*788dup	rs200602841
NM_080911.3(UNG):c.*866AT[9]	rs56185014
NM_080911.3(UNG):c.133-13_133-10dup
NM_080911.3(UNG):c.133-19C>T
NM_080911.3(UNG):c.133-8A>C
NM_080911.3(UNG):c.135C>T (p.Ala45=)
NM_080911.3(UNG):c.138C>A (p.Ile46=)
NM_080911.3(UNG):c.141A>G (p.Pro47=)
NM_080911.3(UNG):c.168G>A (p.Glu56=)
NM_080911.3(UNG):c.189C>G (p.Ser63=)
NM_080911.3(UNG):c.204C>G (p.Ala68=)	rs777436497
NM_080911.3(UNG):c.237C>T (p.Ala79=)
NM_080911.3(UNG):c.273C>G (p.Pro91=)	rs758619136
NM_080911.3(UNG):c.273C>T (p.Pro91=)
NM_080911.3(UNG):c.303C>T (p.His101=)
NM_080911.3(UNG):c.312G>C (p.Gly104=)
NM_080911.3(UNG):c.324A>G (p.Lys108=)
NM_080911.3(UNG):c.339+13A>G
NM_080911.3(UNG):c.339+18C>T
NM_080911.3(UNG):c.36C>T (p.Ser12=)	rs772832695
NM_080911.3(UNG):c.408C>T (p.Thr136=)	rs762887143
NM_080911.3(UNG):c.435+11C>T
NM_080911.3(UNG):c.435+15T>A	rs765672149
NM_080911.3(UNG):c.435+15T>C	rs765672149
NM_080911.3(UNG):c.435+9A>G
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=)
NM_080911.3(UNG):c.495C>T (p.Leu165=)
NM_080911.3(UNG):c.519T>C (p.Val173=)
NM_080911.3(UNG):c.533+17G>T	rs755840023
NM_080911.3(UNG):c.60C>T (p.His20=)
NM_080911.3(UNG):c.622+11G>A
NM_080911.3(UNG):c.622+16C>T	rs2042189211
NM_080911.3(UNG):c.622+19G>C
NM_080911.3(UNG):c.622+20A>T
NM_080911.3(UNG):c.623-10_623-9del
NM_080911.3(UNG):c.623-11C>G
NM_080911.3(UNG):c.623-15C>A
NM_080911.3(UNG):c.623-9T>C
NM_080911.3(UNG):c.654T>C (p.Val218=)
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=)
NM_080911.3(UNG):c.801+16T>C
NM_080911.3(UNG):c.801+18T>C
NM_080911.3(UNG):c.801+19_801+22del
NM_080911.3(UNG):c.802-12G>C
NM_080911.3(UNG):c.802-15C>A
NM_080911.3(UNG):c.802-9C>T
NM_080911.3(UNG):c.819A>G (p.Leu273=)	rs1593326380
NM_080911.3(UNG):c.825G>A (p.Thr275=)	rs765151419
NM_080911.3(UNG):c.895C>T (p.Leu299=)
NM_080911.3(UNG):c.90G>A (p.Gly30=)
NM_080911.3(UNG):c.90G>T (p.Gly30=)	rs766467977
NM_080911.3(UNG):c.924T>A (p.Ile308=)

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