ClinVar Miner

List of variants in gene GNE reported as likely benign

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Gene type:
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Total variants: 48
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HGVS dbSNP
NC_000009.12:g.36223003G>A
NC_000009.12:g.36277137G>A
NM_001128227.3(GNE):c.-10G>A rs73449614
NM_001128227.3(GNE):c.51+17T>G rs144416128
NM_001128227.3(GNE):c.51+63A>G
NM_005476.7(GNE):c.*1021A>G rs10435799
NM_005476.7(GNE):c.*1204T>C rs183365416
NM_005476.7(GNE):c.*1635G>A rs190727651
NM_005476.7(GNE):c.*2056C>T rs183641957
NM_005476.7(GNE):c.*2211C>G rs150978860
NM_005476.7(GNE):c.*2269C>T rs575299401
NM_005476.7(GNE):c.*2415T>A rs143569888
NM_005476.7(GNE):c.*2576A>G rs531142218
NM_005476.7(GNE):c.*277_*279ATA[1] rs140089561
NM_005476.7(GNE):c.*2789G>A rs140396892
NM_005476.7(GNE):c.*30C>G rs540975887
NM_005476.7(GNE):c.*583G>A rs182741472
NM_005476.7(GNE):c.*74G>A rs16933089
NM_005476.7(GNE):c.*937G>A rs191229205
NM_005476.7(GNE):c.-152G>T rs142004500
NM_005476.7(GNE):c.-65G>A rs138897916
NM_005476.7(GNE):c.1233C>T (p.Ala411=) rs1057523203
NM_005476.7(GNE):c.1242T>C (p.Leu414=) rs371881711
NM_005476.7(GNE):c.1245C>A (p.Gly415=) rs140784655
NM_005476.7(GNE):c.1245C>T (p.Gly415=) rs140784655
NM_005476.7(GNE):c.1251G>A (p.Thr417=)
NM_005476.7(GNE):c.1267A>G (p.Ile423Val) rs35638832
NM_005476.7(GNE):c.1281+44G>A rs16933102
NM_005476.7(GNE):c.1281+6A>T rs201025841
NM_005476.7(GNE):c.1293T>A (p.Val431=) rs143485388
NM_005476.7(GNE):c.1311C>T (p.Phe437=) rs1554659051
NM_005476.7(GNE):c.1509C>G (p.Pro503=) rs141172610
NM_005476.7(GNE):c.1633+341G>T
NM_005476.7(GNE):c.165-18A>G rs374105190
NM_005476.7(GNE):c.165-9C>T rs760509369
NM_005476.7(GNE):c.1770C>T (p.Tyr590=) rs111302956
NM_005476.7(GNE):c.1872G>A (p.Ala624=) rs145361930
NM_005476.7(GNE):c.1908G>A (p.Ala636=) rs200812140
NM_005476.7(GNE):c.1934-36T>A rs375573973
NM_005476.7(GNE):c.2086G>T (p.Val696Leu) rs121908627
NM_005476.7(GNE):c.2112C>T (p.Pro704=) rs779967033
NM_005476.7(GNE):c.2118G>A (p.Leu706=) rs1554657933
NM_005476.7(GNE):c.297T>C (p.Leu99=) rs544304534
NM_005476.7(GNE):c.617-260A>C
NM_005476.7(GNE):c.624T>G (p.Asp208Glu) rs35224402
NM_005476.7(GNE):c.765C>T (p.Asp255=) rs775805166
NM_005476.7(GNE):c.804G>A (p.Lys268=) rs141814943
NM_005476.7(GNE):c.843C>T (p.His281=) rs138694766

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