ClinVar Miner

List of variants in gene GNE reported as likely benign for Inclusion Body Myopathy, Recessive

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Gene type:
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Total variants: 21
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HGVS dbSNP
NM_001128227.2(GNE):c.1863C>T (p.Tyr621=) rs111302956
NM_001128227.2(GNE):c.2179G>T (p.Val727Leu) rs121908627
NM_005476.5(GNE):c.*1021A>G rs10435799
NM_005476.5(GNE):c.*1204T>C rs183365416
NM_005476.5(GNE):c.*1635G>A rs190727651
NM_005476.5(GNE):c.*2056C>T rs183641957
NM_005476.5(GNE):c.*2211C>G rs150978860
NM_005476.5(GNE):c.*2269C>T rs575299401
NM_005476.5(GNE):c.*2415T>A rs143569888
NM_005476.5(GNE):c.*2576A>G rs531142218
NM_005476.5(GNE):c.*2789G>A rs140396892
NM_005476.5(GNE):c.*280_*282delATA rs140089561
NM_005476.5(GNE):c.*30C>G rs540975887
NM_005476.5(GNE):c.*583G>A rs182741472
NM_005476.5(GNE):c.*74G>A rs16933089
NM_005476.5(GNE):c.*937G>A rs191229205
NM_005476.5(GNE):c.-152G>T rs142004500
NM_005476.5(GNE):c.-65G>A rs138897916
NM_005476.5(GNE):c.1267A>G (p.Ile423Val) rs35638832
NM_005476.5(GNE):c.1281+6A>T rs201025841
NM_005476.5(GNE):c.1872G>A (p.Ala624=) rs145361930

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