List of variants in gene AKAP9 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_005751.5(AKAP9):c.7275G>A (p.Gln2425=)	rs61757672	0.00298
NM_005751.5(AKAP9):c.6556T>C (p.Ser2186Pro)	rs76177450	0.00250
NM_005751.5(AKAP9):c.10197T>C (p.Thr3399=)	rs143627839	0.00148
NM_005751.5(AKAP9):c.6921A>G (p.Gln2307=)	rs141156177	0.00136
NM_005751.5(AKAP9):c.10767G>A (p.Leu3589=)	rs56198613	0.00111
NM_005751.5(AKAP9):c.6176A>G (p.Glu2059Gly)	rs73226383	0.00070
NM_005751.5(AKAP9):c.10254G>C (p.Gln3418His)	rs61757663	0.00065
NM_005751.5(AKAP9):c.10118C>A (p.Ser3373Tyr)	rs140470576	0.00061
NM_005751.5(AKAP9):c.5246T>C (p.Ile1749Thr)	rs150016098	0.00061
NM_005751.5(AKAP9):c.3580G>A (p.Ala1194Thr)	rs139965373	0.00035
NM_005751.5(AKAP9):c.4825A>C (p.Arg1609=)	rs143473598	0.00033
NM_005751.5(AKAP9):c.9697C>T (p.Arg3233Cys)	rs61757674	0.00026
NM_005751.5(AKAP9):c.10518C>T (p.Thr3506=)	rs377663331	0.00021
NM_005751.5(AKAP9):c.126G>A (p.Thr42=)	rs186969744	0.00010
NM_005751.5(AKAP9):c.11362G>C (p.Val3788Leu)	rs199527737	0.00008
NM_005751.5(AKAP9):c.2477T>C (p.Ile826Thr)	rs534185372	0.00006
NM_005751.5(AKAP9):c.9830T>C (p.Ile3277Thr)	rs144021475	0.00003
NM_005751.5(AKAP9):c.10107T>C (p.Tyr3369=)	rs376961682	0.00002
NM_005751.5(AKAP9):c.4351A>G (p.Met1451Val)	rs1330827109
NM_005751.5(AKAP9):c.5622A>C (p.Thr1874=)
NM_005751.5(AKAP9):c.6366A>C (p.Thr2122=)

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