List of variants in gene CDAN1 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_138477.4(CDAN1):c.2174+20G>A	rs75993383	0.02307
NM_138477.4(CDAN1):c.1967C>G (p.Thr656Ser)	rs139202766	0.00296
NM_138477.4(CDAN1):c.2463G>A (p.Gly821=)	rs139809959	0.00204
NM_138477.4(CDAN1):c.2735C>T (p.Ala912Val)	rs143086237	0.00130
NM_138477.4(CDAN1):c.2164C>T (p.Arg722Cys)	rs140014115	0.00123
NM_138477.4(CDAN1):c.2743T>C (p.Leu915=)	rs149472555	0.00061
NM_138477.4(CDAN1):c.2868C>T (p.Ala956=)	rs150438471	0.00046
NM_138477.4(CDAN1):c.2872C>T (p.Leu958=)	rs764432820	0.00001
NM_138477.4(CDAN1):c.1368-5G>A
NM_138477.4(CDAN1):c.1686C>G (p.Pro562=)
NM_138477.4(CDAN1):c.1821G>A (p.Glu607=)
NM_138477.4(CDAN1):c.2263-6dup
NM_138477.4(CDAN1):c.2433G>A (p.Ser811=)
NM_138477.4(CDAN1):c.2805-3T>C
NM_138477.4(CDAN1):c.3135C>T (p.Asp1045=)	rs146289653
NM_138477.4(CDAN1):c.3147C>A (p.Ser1049=)
NM_138477.4(CDAN1):c.3269-10C>T
NM_138477.4(CDAN1):c.3273A>C (p.Ala1091=)
NM_138477.4(CDAN1):c.3591T>C (p.Asn1197=)
NM_138477.4(CDAN1):c.639C>G (p.Thr213=)
NM_138477.4(CDAN1):c.90+7G>C
NM_138477.4(CDAN1):c.912T>C (p.Leu304=)

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