List of variants in gene FBXO38 reported as benign by Invitae

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_205836.3(FBXO38):c.1619-4G>T	rs11168047	0.42278
NM_205836.3(FBXO38):c.3170+11T>C	rs10051223	0.42229
NM_205836.3(FBXO38):c.1774T>C (p.Ser592Pro)	rs10043775	0.27145
NM_205836.3(FBXO38):c.962+18A>G	rs10077690	0.20380
NM_205836.3(FBXO38):c.2680G>A (p.Ala894Thr)	rs11949133	0.03254
NM_205836.3(FBXO38):c.2654-16T>C	rs147707335	0.02178
NM_205836.3(FBXO38):c.198A>G (p.Leu66=)	rs74863106	0.01529
NM_205836.3(FBXO38):c.593-13A>T	rs61555444	0.00390
NM_205836.3(FBXO38):c.87T>C (p.Tyr29=)	rs77480566	0.00255
NM_205836.3(FBXO38):c.1093+20A>C	rs140611091	0.00034
NM_205836.3(FBXO38):c.504T>C (p.Phe168=)	rs377754520	0.00029
NM_205836.3(FBXO38):c.2985C>T (p.Pro995=)	rs144172824	0.00025
NM_205836.3(FBXO38):c.702A>G (p.Leu234=)	rs144011381	0.00020
NM_205836.3(FBXO38):c.510T>C (p.Asn170=)	rs760368532	0.00012
NM_205836.3(FBXO38):c.1394G>A (p.Arg465His)	rs200187682	0.00010
NM_205836.3(FBXO38):c.1738+8T>A	rs369463389	0.00009
NM_205836.3(FBXO38):c.1527C>T (p.His509=)	rs182585967	0.00004
NM_205836.3(FBXO38):c.2751G>A (p.Val917=)	rs201169649	0.00004
NM_205836.3(FBXO38):c.2858-18A>G	rs376871117	0.00002
NM_205836.3(FBXO38):c.1739-4del
NM_205836.3(FBXO38):c.1739-4dup
NM_205836.3(FBXO38):c.2440G>T (p.Ala814Ser)
NM_205836.3(FBXO38):c.2857+21_2857+23del	rs143121025
NM_205836.3(FBXO38):c.3357C>T (p.Phe1119=)	rs577469242
NM_205836.3(FBXO38):c.731-5dup	rs201558003
NM_205836.3(FBXO38):c.731-6_731-5dup	rs201558003

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