ClinVar Miner

List of variants in gene MYL3 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 93
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HGVS dbSNP gnomAD frequency
NM_000258.3(MYL3):c.307+37A>C rs2227294 0.34149
NM_000258.3(MYL3):c.129+44G>T rs936175 0.30333
NM_000258.3(MYL3):c.*89G>A rs1042973 0.17840
NM_000258.3(MYL3):c.308-257G>A rs1463395 0.12307
NM_000258.3(MYL3):c.482-100C>T rs3729704 0.08920
NC_000003.12:g.46863682T>C rs142106468 0.02371
NM_000258.3(MYL3):c.129+193C>A rs28763895 0.02328
NM_000258.3(MYL3):c.69C>T (p.Pro23=) rs2233264 0.02058
NM_001406938.1(MYL3):c.-6-371G>A rs2233263 0.01935
NM_000258.3(MYL3):c.130-14G>T rs192329378 0.00198
NM_000258.3(MYL3):c.307+86G>A rs561570934 0.00155
NM_000258.3(MYL3):c.81T>C (p.Pro27=) rs147584015 0.00133
NM_000258.3(MYL3):c.-27C>T rs201910884 0.00079
NM_000258.3(MYL3):c.559+6C>T rs199474709 0.00077
NM_000258.3(MYL3):c.482-14C>A rs201780962 0.00048
NM_000258.3(MYL3):c.307+15C>T rs184025552 0.00036
NM_000258.3(MYL3):c.482-17C>T rs201289145 0.00030
NM_000258.3(MYL3):c.307+16G>A rs759754750 0.00029
NM_000258.3(MYL3):c.157+8G>C rs777555567 0.00013
NM_000258.3(MYL3):c.4G>C (p.Ala2Pro) rs148310342 0.00012
NM_000258.3(MYL3):c.559+19G>A rs552393482 0.00012
NM_000258.3(MYL3):c.*13+5G>C rs200422816 0.00011
NM_000258.3(MYL3):c.516G>A (p.Leu172=) rs367761724 0.00008
NM_000258.3(MYL3):c.*9C>T rs202234617 0.00006
NM_000258.3(MYL3):c.420C>T (p.Phe140=) rs201138698 0.00006
NM_000258.2(MYL3):c.-90C>T rs372094875 0.00004
NM_000258.3(MYL3):c.246G>A (p.Ala82=) rs368364468 0.00004
NM_000258.3(MYL3):c.466G>A (p.Val156Met) rs199474707 0.00004
NM_000258.3(MYL3):c.130-10C>T rs374988162 0.00003
NM_000258.3(MYL3):c.154G>A (p.Glu52Lys) rs1355038672 0.00003
NM_000258.3(MYL3):c.477G>A (p.Thr159=) rs148365503 0.00003
NM_000258.3(MYL3):c.91C>T (p.Arg31Cys) rs377026344 0.00003
NM_000258.3(MYL3):c.136T>C (p.Phe46Leu) rs730880953 0.00002
NM_000258.3(MYL3):c.152T>C (p.Ile51Thr) rs749017586 0.00002
NM_000258.3(MYL3):c.219C>T (p.Tyr73=) rs780500137 0.00002
NM_000258.3(MYL3):c.280C>T (p.Arg94Cys) rs730880961 0.00002
NM_000258.3(MYL3):c.461G>A (p.Arg154His) rs104893749 0.00002
NM_000258.3(MYL3):c.530A>G (p.Glu177Gly) rs193922391 0.00002
NM_000258.3(MYL3):c.532G>A (p.Asp178Asn) rs145520567 0.00002
NM_000258.3(MYL3):c.*27G>A rs199474710 0.00001
NM_000258.3(MYL3):c.102G>T (p.Glu34Asp) rs1702010711 0.00001
NM_000258.3(MYL3):c.183C>T (p.Phe61=) rs368118534 0.00001
NM_000258.3(MYL3):c.193C>T (p.Pro65Ser) rs730880960 0.00001
NM_000258.3(MYL3):c.194C>G (p.Pro65Arg) rs730880955 0.00001
NM_000258.3(MYL3):c.220G>A (p.Gly74Arg) rs730880956 0.00001
NM_000258.3(MYL3):c.222G>A (p.Gly74=) rs144543453 0.00001
NM_000258.3(MYL3):c.256A>T (p.Asn86Tyr) rs1257328187 0.00001
NM_000258.3(MYL3):c.26A>G (p.Lys9Arg) rs1025864971 0.00001
NM_000258.3(MYL3):c.281G>A (p.Arg94His) rs199474703 0.00001
NM_000258.3(MYL3):c.381A>C (p.Thr127=) rs758267230 0.00001
NM_000258.3(MYL3):c.427G>A (p.Glu143Lys) rs104893750 0.00001
NM_000258.3(MYL3):c.465C>T (p.His155=) rs147125759 0.00001
NM_000258.3(MYL3):c.482G>A (p.Gly161Asp) rs1057518300 0.00001
NM_000258.3(MYL3):c.501C>T (p.Asp167=) rs552824036 0.00001
NM_000258.3(MYL3):c.517A>G (p.Met173Val) rs199474708 0.00001
NM_000258.3(MYL3):c.73C>T (p.Pro25Ser) rs369256548 0.00001
NM_000258.3(MYL3):c.*13+40G>T rs2106904116
NM_000258.3(MYL3):c.11A>G (p.Lys4Arg) rs727503301
NM_000258.3(MYL3):c.130-322C>A rs77221239
NM_000258.3(MYL3):c.142C>G (p.Pro48Ala) rs2106910525
NM_000258.3(MYL3):c.170C>A (p.Ala57Asp) rs139794067
NM_000258.3(MYL3):c.170C>G (p.Ala57Gly) rs139794067
NM_000258.3(MYL3):c.17C>G (p.Pro6Arg) rs730880959
NM_000258.3(MYL3):c.184G>A (p.Asp62Asn) rs730880954
NM_000258.3(MYL3):c.188G>C (p.Arg63Pro) rs139354105
NM_000258.3(MYL3):c.1_2delinsG (p.Met1fs) rs1702012642
NM_000258.3(MYL3):c.211A>T (p.Ile71Phe)
NM_000258.3(MYL3):c.249G>T (p.Leu83=) rs2106909829
NM_000258.3(MYL3):c.261C>T (p.Pro87=) rs556711370
NM_000258.3(MYL3):c.292A>G (p.Lys98Glu) rs730880957
NM_000258.3(MYL3):c.307+56T>G rs200593962
NM_000258.3(MYL3):c.36T>C (p.Asp12=) rs138567316
NM_000258.3(MYL3):c.36T>G (p.Asp12Glu) rs138567316
NM_000258.3(MYL3):c.380C>G (p.Thr127Arg) rs730880958
NM_000258.3(MYL3):c.411G>T (p.Leu137=) rs2233265
NM_000258.3(MYL3):c.413G>A (p.Arg138Gln) rs1057524652
NM_000258.3(MYL3):c.435T>A (p.Asn145Lys) rs774762882
NM_000258.3(MYL3):c.445A>G (p.Met149Val) rs104893748
NM_000258.3(MYL3):c.447G>T (p.Met149Ile) rs730880162
NM_000258.3(MYL3):c.449G>A (p.Gly150Asp) rs1085307526
NM_000258.3(MYL3):c.451G>A (p.Ala151Thr) rs869025486
NM_000258.3(MYL3):c.454G>A (p.Glu152Lys) rs199474705
NM_000258.3(MYL3):c.456G>T (p.Glu152Asp) rs777855362
NM_000258.3(MYL3):c.457del (p.Leu153fs) rs1064793448
NM_000258.3(MYL3):c.463C>G (p.His155Asp) rs199474706
NM_000258.3(MYL3):c.466G>T (p.Val156Leu) rs199474707
NM_000258.3(MYL3):c.477G>T (p.Thr159=) rs148365503
NM_000258.3(MYL3):c.518T>A (p.Met173Lys) rs730880962
NM_000258.3(MYL3):c.518T>C (p.Met173Thr) rs730880962
NM_000258.3(MYL3):c.549C>T (p.Ile183=) rs963631094
NM_000258.3(MYL3):c.560-30T>C rs760655445
NM_000258.3(MYL3):c.568A>G (p.Lys190Glu) rs1701953031
NM_000258.3(MYL3):c.577A>G (p.Met193Val) rs1701951996

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