ClinVar Miner

List of variants in gene UNC13D reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_199242.3(UNC13D):c.3198A>G (p.Glu1066=) rs7210574 0.49757
NM_199242.3(UNC13D):c.2599A>G (p.Lys867Glu) rs1135688 0.47045
NM_199242.3(UNC13D):c.154-19G>A rs3744009 0.24392
NM_199242.3(UNC13D):c.1596+36A>G rs3744026 0.23763
NM_199242.3(UNC13D):c.1728-48T>C rs3744024 0.23380
NM_199242.3(UNC13D):c.1992+5G>A rs17581728 0.19407
NM_199242.3(UNC13D):c.2299-46C>T rs7212635 0.18407
NM_199242.3(UNC13D):c.117+30G>A rs3744011 0.10282
NM_199242.3(UNC13D):c.754-31C>T rs7226310 0.09910
NM_199242.3(UNC13D):c.1389+36G>A rs74410877 0.08586
NM_199242.3(UNC13D):c.1390-38T>C rs112501005 0.02851
NM_199242.3(UNC13D):c.1744C>T (p.Leu582=) rs75853379 0.02622
NM_199242.3(UNC13D):c.1977C>T (p.Thr659=) rs2290770 0.02469
NM_199242.3(UNC13D):c.262-17G>A rs142996967 0.01903
NM_199242.3(UNC13D):c.1579C>T (p.Arg527Trp) rs75366116 0.01644
NM_199242.3(UNC13D):c.951+13T>G rs140758914 0.01637
NM_199242.3(UNC13D):c.175G>A (p.Ala59Thr) rs9904366 0.01403
NM_199242.3(UNC13D):c.3252T>C (p.His1084=) rs61753922 0.01313
NM_199242.3(UNC13D):c.1992+11T>C rs112501965 0.01262
NM_199242.3(UNC13D):c.904C>T (p.Leu302Phe) rs55661958 0.01066
NM_199242.3(UNC13D):c.2298+15C>T rs112341334 0.00741
NM_199242.3(UNC13D):c.753+3G>A rs116229331 0.00627
NM_199242.3(UNC13D):c.1055+47C>T rs185419295 0.00566
NM_199242.3(UNC13D):c.754-49G>A rs201702634 0.00387
NM_199242.3(UNC13D):c.684-31C>T rs114861309 0.00363
NM_199242.3(UNC13D):c.2335G>A (p.Val779Met) rs113861754 0.00355
NM_199242.3(UNC13D):c.847A>G (p.Ile283Val) rs61754871 0.00194
NM_199242.3(UNC13D):c.1056-13C>T rs141030299 0.00169
NM_199242.3(UNC13D):c.567C>A (p.Ile189=) rs147903551 0.00134
NM_199242.3(UNC13D):c.24G>A (p.Pro8=) rs143320460 0.00095
NM_199242.3(UNC13D):c.99G>A (p.Pro33=) rs147886860 0.00090
NM_199242.3(UNC13D):c.2052C>G (p.Leu684=) rs150861045 0.00070
NM_199242.3(UNC13D):c.3078C>T (p.Pro1026=) rs372034111 0.00056
NM_199242.3(UNC13D):c.2553+5C>G rs201930023 0.00051
NM_199242.3(UNC13D):c.2625+38G>A rs199759320 0.00048
NM_199242.3(UNC13D):c.1228A>C (p.Ile410Leu) rs117221419 0.00040
NM_199242.3(UNC13D):c.811C>T (p.Pro271Ser) rs139564938 0.00020
NM_199242.3(UNC13D):c.114G>A (p.Pro38=) rs755103812 0.00019
NM_199242.3(UNC13D):c.1131C>G (p.Ser377Arg) rs142335129 0.00018
NM_199242.3(UNC13D):c.262-7C>T rs368236546 0.00017
NM_199242.3(UNC13D):c.1014C>T (p.His338=) rs375097777 0.00006
NM_199242.3(UNC13D):c.1156C>T (p.Arg386Trp) rs536336944 0.00005
NM_199242.3(UNC13D):c.2250C>T (p.Ala750=) rs146737486 0.00004
NM_199242.3(UNC13D):c.754-9G>A rs765308578 0.00004
NM_199242.3(UNC13D):c.1447-8C>G rs760322200 0.00003
NM_199242.3(UNC13D):c.271G>A (p.Val91Met) rs374308904 0.00002
NM_199242.3(UNC13D):c.1611G>A (p.Val537=) rs538427767 0.00001
NM_199242.3(UNC13D):c.2370C>T (p.Ala790=) rs747428323 0.00001
NM_199242.3(UNC13D):c.594G>A (p.Ala198=) rs755967157 0.00001
NM_199242.3(UNC13D):c.1024A>G (p.Lys342Glu)
NM_199242.3(UNC13D):c.117+133C>T
NM_199242.3(UNC13D):c.118-321C>G
NM_199242.3(UNC13D):c.118-326G>A
NM_199242.3(UNC13D):c.1849-39G>T
NM_199242.3(UNC13D):c.2046C>T (p.Arg682=) rs139837456
NM_199242.3(UNC13D):c.2364G>A (p.Glu788=)
NM_199242.3(UNC13D):c.2448-8dup rs3217698
NM_199242.3(UNC13D):c.2554-4C>T
NM_199242.3(UNC13D):c.261+26C>G rs3744008
NM_199242.3(UNC13D):c.279C>T (p.Pro93=) rs3744007
NM_199242.3(UNC13D):c.2954+431_2954+432del
NM_199242.3(UNC13D):c.2954+432del
NM_199242.3(UNC13D):c.2955-9T>G
NM_199242.3(UNC13D):c.3147del (p.Asn1050fs) rs1048876742
NM_199242.3(UNC13D):c.3270G>T (p.Pro1090=)
NM_199242.3(UNC13D):c.499G>A (p.Glu167Lys)
NM_199242.3(UNC13D):c.570-9T>A
NM_199242.3(UNC13D):c.888G>C (p.Pro296=) rs7223416

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