ClinVar Miner

List of variants studied for Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations by Illumina Laboratory Services, Illumina

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_033629.6(TREX1):c.531= (p.Tyr177=) rs11797 0.37009
NM_033629.6(TREX1):c.-68T>C rs3135941 0.13944
NM_033629.6(TREX1):c.912G>A (p.Leu304=) rs3135945 0.04049
NM_033629.6(TREX1):c.*37T>C rs3135946 0.03909
NM_033629.6(TREX1):c.-60C>T rs2279076 0.00673
NM_033629.6(TREX1):c.462T>C (p.Asp154=) rs3135944 0.00576
NM_033629.6(TREX1):c.198G>A (p.Lys66=) rs3135943 0.00490
NM_033629.4(TREX1):c.-515T>C rs148393533 0.00332
NM_033629.4(TREX1):c.-127G>C rs577465983 0.00213
NM_033629.6(TREX1):c.797A>G (p.Glu266Gly) rs55999987 0.00175
NM_033629.4(TREX1):c.-117C>T rs548710061 0.00113
NM_033629.6(TREX1):c.183G>A (p.Pro61=) rs55852466 0.00034
NM_033629.4(TREX1):c.-199A>G rs767364235 0.00015
NM_033629.6(TREX1):c.312G>C (p.Leu104=) rs56162833 0.00010
NM_033629.6(TREX1):c.651G>A (p.Arg217=) rs140199177 0.00007
NM_033629.6(TREX1):c.346C>G (p.Pro116Ala) rs761651331 0.00006
NM_033629.4(TREX1):c.-287C>T rs377157141 0.00005
NM_033629.6(TREX1):c.473C>T (p.Ala158Val) rs762011967 0.00004
NM_033629.6(TREX1):c.649C>T (p.Arg217Trp) rs201068640 0.00003
NM_033629.6(TREX1):c.-100C>T rs886058623 0.00002
NM_033629.6(TREX1):c.9G>A (p.Ser3=) rs762687506 0.00002
NM_033629.6(TREX1):c.418A>G (p.Met140Val) rs761526437 0.00001
NM_033629.6(TREX1):c.554G>A (p.Arg185His) rs767157848 0.00001
NM_033629.6(TREX1):c.846A>G (p.Leu282=) rs374232562 0.00001
NM_033629.4(TREX1):c.-206G>T rs886058622
NM_033629.4(TREX1):c.-510delC rs3135939
NM_033629.6(TREX1):c.-50CTGC[4] rs371036312
NM_033629.6(TREX1):c.394C>G (p.Pro132Ala) rs200510205
NM_033629.6(TREX1):c.536T>C (p.Leu179Pro) rs886058625
NM_033629.6(TREX1):c.803G>C (p.Arg268Thr) rs2040380664

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