List of variants in gene AKAP9 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_005751.5(AKAP9):c.2425A>G (p.Ile809Val)	rs144615758	0.00298
NM_005751.5(AKAP9):c.10858A>G (p.Ile3620Val)	rs142729919	0.00296
NM_005751.5(AKAP9):c.11098-13T>G	rs76709221	0.00235
NM_005751.5(AKAP9):c.288G>T (p.Glu96Asp)	rs34953651	0.00112
NM_005751.5(AKAP9):c.9358+11T>C	rs199714035	0.00101
NM_005751.5(AKAP9):c.6508-20A>T	rs374874284	0.00079
NM_005751.5(AKAP9):c.5246T>C (p.Ile1749Thr)	rs150016098	0.00061
NM_005751.5(AKAP9):c.4163C>T (p.Ser1388Leu)	rs143565222	0.00034
NM_005751.5(AKAP9):c.8161-7G>A	rs202218770	0.00019
NM_005751.5(AKAP9):c.7212C>T (p.Thr2404=)	rs146854871	0.00014
NM_005751.5(AKAP9):c.610G>A (p.Asp204Asn)	rs148920964	0.00011
NM_005751.5(AKAP9):c.261A>G (p.Leu87=)	rs150736347	0.00006
NM_005751.5(AKAP9):c.6681A>G (p.Gln2227=)	rs745898364	0.00006
NM_005751.5(AKAP9):c.1044A>C (p.Leu348=)	rs747912745	0.00001
NM_005751.5(AKAP9):c.8052A>G (p.Glu2684=)	rs878854810	0.00001
NM_005751.5(AKAP9):c.11682G>A (p.Gln3894=)	rs769718964
NM_005751.5(AKAP9):c.4918-10dup	rs755283199

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