Variants in gene CUL7 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_014780.5(CUL7):c.1846A>G (p.Ser616Gly)	rs7774330	0.01270
NM_014780.5(CUL7):c.4914C>T (p.Asp1638=)	rs61731584	0.00197
NM_014780.5(CUL7):c.861G>A (p.Gly287=)	rs61750322	0.00140
NM_014780.5(CUL7):c.3768C>T (p.Ser1256=)	rs138763036	0.00111
NM_014780.5(CUL7):c.4659G>A (p.Glu1553=)	rs139243761	0.00107
NM_014780.5(CUL7):c.4935C>T (p.Ser1645=)	rs116910528	0.00049
NM_014780.5(CUL7):c.3876C>T (p.Ile1292=)	rs147056081	0.00046
NM_014780.5(CUL7):c.1030G>A (p.Ala344Thr)	rs183119565	0.00042
NM_014780.5(CUL7):c.4731C>T (p.Ala1577=)	rs141716467	0.00038
NM_014780.5(CUL7):c.1542G>T (p.Gln514His)	rs146808129	0.00036
NM_014780.5(CUL7):c.3432G>A (p.Thr1144=)	rs144556973	0.00036
NM_014780.5(CUL7):c.687G>A (p.Thr229=)	rs192945321	0.00019
NM_014780.5(CUL7):c.2603A>G (p.Asn868Ser)	rs149360738	0.00007
NM_014780.5(CUL7):c.1168GAG[1] (p.Glu391del)	rs372224208
NM_014780.5(CUL7):c.2229C>G (p.Ala743=)	rs188565648

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