ClinVar Miner

List of variants in gene combination EMG1, LPCAT3 reported as uncertain significance for not specified

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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_005768.6(LPCAT3):c.340G>A (p.Val114Ile) rs142589366 0.00035
NM_005768.6(LPCAT3):c.320T>C (p.Met107Thr) rs139480947 0.00027
NM_005768.6(LPCAT3):c.992C>T (p.Thr331Ile) rs200922476 0.00015
NM_005768.6(LPCAT3):c.346A>G (p.Thr116Ala) rs367654948 0.00007
NM_005768.6(LPCAT3):c.310C>G (p.Leu104Val) rs376479324 0.00005
NM_005768.6(LPCAT3):c.1455G>C (p.Lys485Asn) rs1405137368 0.00003
NM_005768.6(LPCAT3):c.1217C>T (p.Thr406Ile) rs1035421832 0.00002
NM_005768.6(LPCAT3):c.1033G>C (p.Val345Leu) rs372779694 0.00001
NM_005768.6(LPCAT3):c.1061A>G (p.Lys354Arg) rs782278519 0.00001
NM_005768.6(LPCAT3):c.1381T>A (p.Phe461Ile) rs781810040 0.00001
NM_005768.6(LPCAT3):c.1402A>G (p.Ile468Val) rs782718258 0.00001
NM_005768.6(LPCAT3):c.214C>T (p.Leu72Phe) rs781806022 0.00001
NM_005768.6(LPCAT3):c.1001T>C (p.Ile334Thr) rs1565596659
NM_005768.6(LPCAT3):c.1024A>C (p.Asn342His) rs1555153591
NM_005768.6(LPCAT3):c.1379T>C (p.Ile460Thr) rs921327898
NM_005768.6(LPCAT3):c.1428G>A (p.Met476Ile)
NM_005768.6(LPCAT3):c.278C>T (p.Ser93Phe)
NM_005768.6(LPCAT3):c.314G>A (p.Arg105Gln)
NM_005768.6(LPCAT3):c.326G>A (p.Arg109His) rs782492797
NM_005768.6(LPCAT3):c.403G>A (p.Gly135Ser)
NM_005768.6(LPCAT3):c.487G>A (p.Gly163Arg)
NM_005768.6(LPCAT3):c.536G>C (p.Arg179Pro) rs782324010
NM_005768.6(LPCAT3):c.817A>G (p.Met273Val) rs1555153647
NM_005768.6(LPCAT3):c.940G>A (p.Asp314Asn)

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