ClinVar Miner

List of variants in gene AGAP1 reported as benign for not provided

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_001037131.3(AGAP1):c.1051-30574_1051-30571dup rs142341634 0.14555
NM_001037131.3(AGAP1):c.2382C>T (p.Asp794=) rs73996547 0.01736
NM_001037131.3(AGAP1):c.504G>A (p.Thr168=) rs144494543 0.00315
NM_001037131.3(AGAP1):c.375A>G (p.Glu125=) rs144424571 0.00170
NM_001037131.3(AGAP1):c.1026C>T (p.Ser342=)
NM_001037131.3(AGAP1):c.1051-20T>C
NM_001037131.3(AGAP1):c.1156-7del
NM_001037131.3(AGAP1):c.1218A>G (p.Pro406=)
NM_001037131.3(AGAP1):c.132C>T (p.Asn44=)
NM_001037131.3(AGAP1):c.1484-14C>T
NM_001037131.3(AGAP1):c.163+18T>C
NM_001037131.3(AGAP1):c.1645+13C>T
NM_001037131.3(AGAP1):c.1892-4G>A
NM_001037131.3(AGAP1):c.1984C>A (p.Arg662=)
NM_001037131.3(AGAP1):c.1996C>T (p.Leu666=)
NM_001037131.3(AGAP1):c.2011G>A (p.Val671Ile)
NM_001037131.3(AGAP1):c.2114+8C>T
NM_001037131.3(AGAP1):c.223-14C>T
NM_001037131.3(AGAP1):c.2262C>T (p.His754=)
NM_001037131.3(AGAP1):c.2274C>T (p.Asp758=)
NM_001037131.3(AGAP1):c.2313G>A (p.Thr771=)
NM_001037131.3(AGAP1):c.2370+13C>T
NM_001037131.3(AGAP1):c.2387C>T (p.Thr796Met)
NM_001037131.3(AGAP1):c.2415T>G (p.Ala805=)
NM_001037131.3(AGAP1):c.2478C>T (p.Cys826=)
NM_001037131.3(AGAP1):c.2494G>A (p.Val832Met)
NM_001037131.3(AGAP1):c.2511T>C (p.Pro837=)
NM_001037131.3(AGAP1):c.393G>T (p.Ala131=)
NM_001037131.3(AGAP1):c.651T>C (p.Asn217=)
NM_001037131.3(AGAP1):c.738A>G (p.Leu246=)
NM_001037131.3(AGAP1):c.849A>G (p.Pro283=)
NM_001037131.3(AGAP1):c.880C>A (p.Arg294=)
NM_001037131.3(AGAP1):c.957C>T (p.Thr319=)
NM_001037131.3(AGAP1):c.958T>C (p.Ser320Pro)

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