ClinVar Miner

List of variants in gene ATRIP, ATRIP-TREX1, TREX1 studied for Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations

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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_130384.3(ATRIP):c.*1632= rs11797 0.37009
NM_130384.3(ATRIP):c.*714T>C rs3135941 0.13734
NM_033629.6(TREX1):c.912G>A (p.Leu304=) rs3135945 0.04049
NM_130384.3(ATRIP):c.*2083T>C rs3135946 0.03909
NM_130384.3(ATRIP):c.*722C>T rs2279076 0.00673
NM_033629.6(TREX1):c.462T>C (p.Asp154=) rs3135944 0.00613
NM_033629.6(TREX1):c.198G>A (p.Lys66=) rs3135943 0.00490
NM_130384.3(ATRIP):c.*267T>C rs148393533 0.00332
NM_130384.3(ATRIP):c.*655G>C rs577465983 0.00222
NM_033629.6(TREX1):c.797A>G (p.Glu266Gly) rs55999987 0.00184
NM_130384.3(ATRIP):c.*665C>T rs548710061 0.00108
NM_033629.6(TREX1):c.183G>A (p.Pro61=) rs55852466 0.00034
NM_033629.6(TREX1):c.341G>A (p.Arg114His) rs72556554 0.00030
NM_130384.3(ATRIP):c.*583A>G rs767364235 0.00017
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_130384.3(ATRIP):c.*495C>T rs377157141 0.00006
NM_033629.6(TREX1):c.473C>T (p.Ala158Val) rs762011967 0.00004
NM_033629.6(TREX1):c.-26-1G>A rs749323787 0.00003
NM_033629.6(TREX1):c.649C>T (p.Arg217Trp) rs201068640 0.00003
NM_130384.3(ATRIP):c.*682C>T rs886058623 0.00002
NM_033629.6(TREX1):c.418A>G (p.Met140Val) rs761526437 0.00001
NM_033629.6(TREX1):c.846A>G (p.Leu282=) rs374232562 0.00001
NM_033629.6(TREX1):c.9G>A (p.Ser3=) rs762687506 0.00001
NM_033629.6(TREX1):c.236_243dup (p.Ser82fs) rs1331920811
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.554G>A (p.Arg185His) rs767157848
NM_033629.6(TREX1):c.621_622del (p.Ile207fs) rs781199890
NM_033629.6(TREX1):c.703_706dup (p.Thr236fs) rs1560113283
NM_033629.6(TREX1):c.703dup (p.Val235fs) rs1553820434
NM_033629.6(TREX1):c.803G>C (p.Arg268Thr) rs2040380664
NM_033629.6(TREX1):c.814del (p.Asp272fs) rs2107265386
NM_130384.3(ATRIP):c.*272del rs3135939
NM_130384.3(ATRIP):c.*576G>T rs886058622
NM_130384.3(ATRIP):c.*732CTGC[4] rs371036312

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