ClinVar Miner

List of variants reported as benign for Progressive myositis ossificans

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_001111067.4(ACVR1):c.690G>A (p.Glu230=) rs1146031 0.91655
NM_001111067.4(ACVR1):c.68-25T>C rs1866885 0.75665
NM_001111067.4(ACVR1):c.270C>T (p.Ala90=) rs2227861 0.62210
NM_001111067.4(ACVR1):c.*686T>C rs12997 0.45193
NM_001111067.4(ACVR1):c.*138G>A rs2228948 0.16631
NM_001111067.4(ACVR1):c.-53C>T rs73966130 0.04478
NM_001111067.4(ACVR1):c.*791A>T rs74392193 0.01967
NM_001111067.4(ACVR1):c.1513T>C (p.Leu505=) rs3738927 0.01961
NM_001111067.4(ACVR1):c.1131C>T (p.Gly377=) rs56189710 0.01889
NM_001111067.4(ACVR1):c.*45G>T rs12936 0.01869
NM_001111067.4(ACVR1):c.643+7C>T rs12105152 0.01446
NM_001111067.4(ACVR1):c.44C>G (p.Ala15Gly) rs13406336 0.00586
NM_001111067.4(ACVR1):c.*358G>A rs79598188 0.00522
NM_001111067.4(ACVR1):c.1506C>T (p.Leu502=) rs55788041 0.00218
NM_001111067.4(ACVR1):c.-182-10C>T rs186304210 0.00135
NM_001111067.4(ACVR1):c.-13A>G rs113455580 0.00118
NM_001111067.4(ACVR1):c.1086C>A (p.Ser362=) rs149498219 0.00076
NM_001111067.4(ACVR1):c.*762A>G rs112908089 0.00051
NM_001111067.4(ACVR1):c.141C>G (p.His47Gln) rs34056189 0.00030
NM_001111067.4(ACVR1):c.99C>T (p.Tyr33=) rs201453468 0.00026
NM_001111067.4(ACVR1):c.*47C>T rs55667327 0.00020
NM_001111067.4(ACVR1):c.*183G>A rs113598201 0.00009
NM_001111067.4(ACVR1):c.484G>A (p.Val162Met) rs201452185 0.00009
NM_001111067.4(ACVR1):c.450A>G (p.Lys150=) rs774878576 0.00005
NM_001111067.4(ACVR1):c.-183+919A>G rs374473767 0.00003
NM_001111067.4(ACVR1):c.*152G>A rs373670847 0.00001

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