ClinVar Miner

List of variants in gene MYL3 reported as likely benign by Color Diagnostics, LLC DBA Color Health

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_000258.3(MYL3):c.4G>C (p.Ala2Pro) rs148310342 0.00012
NM_000258.3(MYL3):c.516G>A (p.Leu172=) rs367761724 0.00008
NM_000258.3(MYL3):c.420C>T (p.Phe140=) rs201138698 0.00006
NM_000258.3(MYL3):c.552C>T (p.Asn184=) rs140829951 0.00006
NM_000258.3(MYL3):c.399C>T (p.Phe133=) rs112992334 0.00005
NM_000258.3(MYL3):c.158-10C>T rs765419653 0.00004
NM_000258.3(MYL3):c.246G>A (p.Ala82=) rs368364468 0.00004
NM_000258.3(MYL3):c.477G>A (p.Thr159=) rs148365503 0.00003
NM_000258.3(MYL3):c.92G>A (p.Arg31His) rs199639940 0.00003
NM_000258.3(MYL3):c.105C>T (p.Val35=) rs771114109 0.00002
NM_000258.3(MYL3):c.219C>T (p.Tyr73=) rs780500137 0.00002
NM_000258.3(MYL3):c.360C>T (p.His120=) rs1314822874 0.00002
NM_000258.3(MYL3):c.532G>A (p.Asp178Asn) rs145520567 0.00002
NM_000258.3(MYL3):c.183C>T (p.Phe61=) rs368118534 0.00001
NM_000258.3(MYL3):c.222G>A (p.Gly74=) rs144543453 0.00001
NM_000258.3(MYL3):c.247C>T (p.Leu83=) rs1246506798 0.00001
NM_000258.3(MYL3):c.27G>A (p.Lys9=) rs994017710 0.00001
NM_000258.3(MYL3):c.30G>A (p.Lys10=) rs779002620 0.00001
NM_000258.3(MYL3):c.426G>A (p.Lys142=) rs1435096286 0.00001
NM_000258.3(MYL3):c.429G>A (p.Glu143=) rs746210438 0.00001
NM_000258.3(MYL3):c.435T>C (p.Asn145=) rs774762882 0.00001
NM_000258.3(MYL3):c.465C>T (p.His155=) rs147125759 0.00001
NM_000258.3(MYL3):c.483T>G (p.Gly161=) rs1345959283 0.00001
NM_000258.3(MYL3):c.501C>T (p.Asp167=) rs552824036 0.00001
NM_000258.3(MYL3):c.507G>A (p.Val169=) rs1166390418 0.00001
NM_000258.3(MYL3):c.555T>C (p.Tyr185=) rs769009588 0.00001
NM_000258.3(MYL3):c.6C>A (p.Ala2=) rs971197044 0.00001
NM_000258.3(MYL3):c.130-4T>G rs1354158647
NM_000258.3(MYL3):c.157+3G>A rs1701986723
NM_000258.3(MYL3):c.158-8C>T rs937857201
NM_000258.3(MYL3):c.165G>A (p.Lys55=) rs397516277
NM_000258.3(MYL3):c.21G>A (p.Glu7=) rs1559520953
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.477G>T (p.Thr159=) rs148365503
NM_000258.3(MYL3):c.514T>C (p.Leu172=) rs1390485854
NM_000258.3(MYL3):c.546C>T (p.Cys182=) rs1701955108
NM_000258.3(MYL3):c.549C>T (p.Ile183=) rs963631094
NM_000258.3(MYL3):c.560-15_560-14del rs1319190482
NM_000258.3(MYL3):c.560-19_560-16del
NM_000258.3(MYL3):c.567G>A (p.Val189=) rs1701953062
NM_000258.3(MYL3):c.582C>T (p.Ser194=) rs1701951849
NM_000258.3(MYL3):c.61C>G (p.Pro21Ala) rs779557153
NM_000258.3(MYL3):c.96T>A (p.Pro32=) rs886058582

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