ClinVar Miner

List of variants in gene CCDC40 reported as benign by Invitae

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_017950.4(CCDC40):c.1123A>C (p.Lys375Gln) rs61734951
NM_017950.4(CCDC40):c.1131C>T (p.Cys377=) rs74692882
NM_017950.4(CCDC40):c.1132G>A (p.Ala378Thr) rs116795025
NM_017950.4(CCDC40):c.1144G>A (p.Glu382Lys) rs2289532
NM_017950.4(CCDC40):c.1220T>C (p.Ile407Thr) rs141185078
NM_017950.4(CCDC40):c.1275C>T (p.Ala425=) rs145013523
NM_017950.4(CCDC40):c.1303G>A (p.Glu435Lys) rs62000409
NM_017950.4(CCDC40):c.1338C>T (p.Leu446=) rs61734950
NM_017950.4(CCDC40):c.1372G>A (p.Ala458Thr) rs372976809
NM_017950.4(CCDC40):c.1449C>T (p.Thr483=) rs116824266
NM_017950.4(CCDC40):c.1466G>T (p.Ser489Ile) rs61739354
NM_017950.4(CCDC40):c.1531G>A (p.Glu511Lys) rs59978698
NM_017950.4(CCDC40):c.1673C>G (p.Thr558Arg) rs191736683
NM_017950.4(CCDC40):c.1806+8C>T rs182104049
NM_017950.4(CCDC40):c.180G>A (p.Ala60=) rs185006459
NM_017950.4(CCDC40):c.1889_1890delinsTG (p.Ala630Val) rs386799737
NM_017950.4(CCDC40):c.2255T>C (p.Leu752Pro) rs117203086
NM_017950.4(CCDC40):c.2336G>A (p.Arg779His) rs183809462
NM_017950.4(CCDC40):c.2387C>G (p.Ala796Gly) rs139435501
NM_017950.4(CCDC40):c.2604C>T (p.Phe868=) rs61749027
NM_017950.4(CCDC40):c.2608C>T (p.Arg870Cys) rs61749025
NM_017950.4(CCDC40):c.2682G>A (p.Ala894=) rs4889815
NM_017950.4(CCDC40):c.2784C>T (p.Ile928=) rs118143944
NM_017950.4(CCDC40):c.2785G>A (p.Gly929Ser) rs59896146
NM_017950.4(CCDC40):c.2868G>A (p.Lys956=) rs1982243
NM_017950.4(CCDC40):c.2892G>A (p.Ala964=) rs146360951
NM_017950.4(CCDC40):c.2900G>T (p.Arg967Leu) rs61686936
NM_017950.4(CCDC40):c.2958C>T (p.Leu986=) rs78945041
NM_017950.4(CCDC40):c.3066A>G (p.Thr1022=) rs534912798
NM_017950.4(CCDC40):c.3349G>A (p.Glu1117Lys) rs145595957
NM_017950.4(CCDC40):c.334A>G (p.Thr112Ala) rs201709592
NM_017950.4(CCDC40):c.3408C>T (p.Leu1136=) rs186591691
NM_017950.4(CCDC40):c.3424T>C (p.Ser1142Pro) rs148900528
NM_017950.4(CCDC40):c.504G>A (p.Pro168=) rs74000351
NM_017950.4(CCDC40):c.507G>A (p.Ser169=) rs2885349
NM_017950.4(CCDC40):c.630C>T (p.Ser210=) rs117419007
NM_017950.4(CCDC40):c.631G>A (p.Asp211Asn) rs150615436
NM_017950.4(CCDC40):c.648C>T (p.Asp216=) rs375350606
NM_017950.4(CCDC40):c.850G>C (p.Asp284His) rs201042940
NM_017950.4(CCDC40):c.946G>A (p.Ala316Thr) rs61998241

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