ClinVar Miner

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

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Total variants: 35
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HGVS dbSNP gnomAD frequency
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.1056-13C>T rs141030299 0.00169
NM_199242.3(UNC13D):c.567C>A (p.Ile189=) rs147903551 0.00134
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.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.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.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.2554-4C>T
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.3270G>T (p.Pro1090=)
NM_199242.3(UNC13D):c.570-9T>A

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