ClinVar Miner

List of variants in gene AKAP9 reported as benign for not provided

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Total variants: 49
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HGVS dbSNP
GRCh37/hg19 7q21.2(chr7:91572749-91691565)x3
GRCh37/hg19 7q21.2(chr7:91572749-91700267)x3
GRCh37/hg19 7q21.2(chr7:91575417-91691565)x3
GRCh37/hg19 7q21.2(chr7:91575417-91694743)x3
GRCh37/hg19 7q21.2(chr7:91707197-91719608)x0
NC_000007.14:g.92071328_92071329del
NM_005751.4(AKAP9):c.-285C>T
NM_005751.4(AKAP9):c.10608-38G>A
NM_005751.4(AKAP9):c.10845G>A (p.Lys3615=) rs138739292
NM_005751.4(AKAP9):c.11097+221A>T
NM_005751.4(AKAP9):c.11416+222A>G
NM_005751.4(AKAP9):c.11417-143T>G
NM_005751.4(AKAP9):c.11417-301C>G
NM_005751.4(AKAP9):c.11546+138A>G
NM_005751.4(AKAP9):c.11546+185C>T
NM_005751.4(AKAP9):c.11546+321T>C
NM_005751.4(AKAP9):c.11546+58T>A
NM_005751.4(AKAP9):c.3223T>C (p.Leu1075=) rs143712699
NM_005751.4(AKAP9):c.3246A>G (p.Ser1082=) rs760173622
NM_005751.4(AKAP9):c.3533-161G>T
NM_005751.4(AKAP9):c.3613-178A>G
NM_005751.4(AKAP9):c.3613-291G>C
NM_005751.4(AKAP9):c.3752-133C>T
NM_005751.4(AKAP9):c.4149-59C>G
NM_005751.4(AKAP9):c.4338+193G>C
NM_005751.4(AKAP9):c.4339-41T>G
NM_005751.4(AKAP9):c.4692+279G>A
NM_005751.4(AKAP9):c.4693-180G>A
NM_005751.4(AKAP9):c.48+154C>A
NM_005751.4(AKAP9):c.49-21G>A
NM_005751.4(AKAP9):c.5059-129C>A
NM_005751.4(AKAP9):c.510G>C (p.Glu170Asp) rs144888041
NM_005751.4(AKAP9):c.5162+318G>A
NM_005751.4(AKAP9):c.5368+280T>C
NM_005751.4(AKAP9):c.5369-251_5369-250insA
NM_005751.4(AKAP9):c.5602-117A>G
NM_005751.4(AKAP9):c.576+307G>A
NM_005751.4(AKAP9):c.5977+146G>T
NM_005751.4(AKAP9):c.6507+259G>A
NM_005751.4(AKAP9):c.6508-239C>T
NM_005751.4(AKAP9):c.6508-312A>C
NM_005751.4(AKAP9):c.6765+303C>G
NM_005751.4(AKAP9):c.6921A>G (p.Gln2307=) rs141156177
NM_005751.4(AKAP9):c.6946-174T>C
NM_005751.4(AKAP9):c.8020-45A>G
NM_005751.4(AKAP9):c.931-161G>C
NM_005751.4(AKAP9):c.931-178T>G
NM_005751.4(AKAP9):c.9729+266G>A
NM_005751.4(AKAP9):c.9730-309G>C

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