List of variants in gene CUL3 reported as likely benign for Autosomal dominant pseudohypoaldosteronism type 1

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_003590.5(CUL3):c.3531_3532del	rs10612010	0.01684
NM_003590.5(CUL3):c.*3156A>G	rs78383940	0.01631
NM_003590.5(CUL3):c.1581A>T (p.Ala527=)	rs41373148	0.01485
NM_003590.5(CUL3):c.2052C>T (p.Ser684=)	rs61743301	0.01372
NM_003590.5(CUL3):c.*1872G>C	rs140669610	0.00756
NM_003590.5(CUL3):c.*3463T>C	rs76433087	0.00570
NM_003590.5(CUL3):c.*2923A>C	rs73077720	0.00490
NM_003590.5(CUL3):c.*2945G>C	rs41529948	0.00430
NM_003590.5(CUL3):c.2029+14T>C	rs201363693	0.00183
NM_003590.5(CUL3):c.*2130A>G	rs555995940	0.00154
NM_003590.5(CUL3):c.*2912T>C	rs567860520	0.00149
NM_003590.5(CUL3):c.*2272T>C	rs556914502	0.00132
NM_003590.5(CUL3):c.*1403A>C	rs575153722	0.00108
NM_003590.5(CUL3):c.*3753T>C	rs558805673	0.00068
NM_003590.5(CUL3):c.*294A>G	rs532967850	0.00067
NM_003590.5(CUL3):c.883+13G>C	rs147823056	0.00061
NM_003590.5(CUL3):c.*896G>C	rs141660429	0.00060
NM_003590.5(CUL3):c.264+9C>T	rs200018000	0.00039
NM_003590.5(CUL3):c.*89A>T	rs192166927	0.00022
NM_003590.5(CUL3):c.693A>C (p.Ser231=)	rs181190157	0.00011
NM_003590.5(CUL3):c.*2863T>G	rs536790634	0.00004
NM_003590.5(CUL3):c.600C>G (p.Val200=)	rs561338665	0.00001
NM_003590.5(CUL3):c.1245_1249del	rs144788294
NM_003590.5(CUL3):c.*1483C>G	rs79297951
NM_003590.5(CUL3):c.1934_1937del	rs533374759
NM_003590.5(CUL3):c.*2117dup	rs572505388
NM_003590.5(CUL3):c.265_269del	rs527449132
NM_003590.5(CUL3):c.1708-14del	rs777017393

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