ClinVar Miner

List of variants in gene MYL3 reported as uncertain significance by GeneDx

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Total variants: 38
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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.466G>A (p.Val156Met) rs199474707 0.00004
NM_000258.3(MYL3):c.154G>A (p.Glu52Lys) rs1355038672 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.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.102G>T (p.Glu34Asp) rs1702010711 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.256A>T (p.Asn86Tyr) rs1257328187 0.00001
NM_000258.3(MYL3):c.26A>G (p.Lys9Arg) rs1025864971 0.00001
NM_000258.3(MYL3):c.482G>A (p.Gly161Asp) rs1057518300 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.11A>G (p.Lys4Arg) rs727503301
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.292A>G (p.Lys98Glu) rs730880957
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.413G>A (p.Arg138Gln) rs1057524652
NM_000258.3(MYL3):c.435T>A (p.Asn145Lys) rs774762882
NM_000258.3(MYL3):c.449G>A (p.Gly150Asp) rs1085307526
NM_000258.3(MYL3):c.456G>T (p.Glu152Asp) rs777855362
NM_000258.3(MYL3):c.466G>T (p.Val156Leu) rs199474707
NM_000258.3(MYL3):c.518T>C (p.Met173Thr) rs730880962
NM_000258.3(MYL3):c.568A>G (p.Lys190Glu) rs1701953031
NM_000258.3(MYL3):c.577A>G (p.Met193Val) rs1701951996

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