ClinVar Miner

List of variants in gene MEF2C reported as likely benign for not specified

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_002397.5(MEF2C):c.811-12G>A rs149706617 0.00064
NM_002397.5(MEF2C):c.180C>T (p.Thr60=) rs773278207 0.00010
NM_002397.5(MEF2C):c.258+7G>C rs372739987 0.00010
NM_002397.5(MEF2C):c.363C>T (p.Asn121=) rs186648089 0.00008
NM_002397.5(MEF2C):c.780A>G (p.Pro260=) rs776117674 0.00008
NM_002397.5(MEF2C):c.258+10C>T rs563149132 0.00004
NM_002397.5(MEF2C):c.312C>T (p.Asp104=) rs587781034 0.00004
NM_002397.5(MEF2C):c.871T>C (p.Leu291=) rs747980554 0.00004
NM_002397.5(MEF2C):c.615G>A (p.Thr205=) rs776496777 0.00002
NM_002397.5(MEF2C):c.810+10A>T rs587783748 0.00002
NM_002397.5(MEF2C):c.834+16G>A rs760064638 0.00002
NM_002397.5(MEF2C):c.1021G>A (p.Ala341Thr) rs797045703 0.00001
NM_002397.5(MEF2C):c.1086C>A (p.Ala362=) rs1057521169 0.00001
NM_002397.5(MEF2C):c.132G>A (p.Ala44=) rs776920242 0.00001
NM_002397.5(MEF2C):c.402+18C>T rs759365719 0.00001
NM_002397.5(MEF2C):c.402+75G>T rs997329230 0.00001
NM_002397.5(MEF2C):c.861G>A (p.Ser287=) rs185655344 0.00001
NM_002397.5(MEF2C):c.-143+11C>T rs1554055657
NM_002397.5(MEF2C):c.-143+17T>A rs1267825119
NM_002397.5(MEF2C):c.-43A>T rs978491338
NM_002397.5(MEF2C):c.129T>C (p.Ile43=) rs1323101986
NM_002397.5(MEF2C):c.1375A>G (p.Ser459Gly) rs1554098520
NM_002397.5(MEF2C):c.1392C>T (p.Arg464=) rs1554098511
NM_002397.5(MEF2C):c.456C>T (p.His152=) rs1554112204
NM_002397.5(MEF2C):c.527C>A (p.Ser176Tyr) rs1057521189
NM_002397.5(MEF2C):c.72G>A (p.Arg24=) rs1057522729
NM_002397.5(MEF2C):c.965-6_965-2del rs1064795146

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