ClinVar Miner

List of variants in gene DCLRE1C reported as uncertain significance for not provided

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_001033855.3(DCLRE1C):c.1284A>C (p.Lys428Asn) rs113870881 0.00220
NM_001033855.3(DCLRE1C):c.1101A>G (p.Pro367=) rs143782439 0.00085
NM_001033855.3(DCLRE1C):c.985T>A (p.Leu329Met) rs41299658 0.00071
NM_001033855.3(DCLRE1C):c.419C>T (p.Ala140Val) rs41297016 0.00056
NM_001033855.3(DCLRE1C):c.420G>A (p.Ala140=) rs146832860 0.00015
NM_001033855.3(DCLRE1C):c.1952T>C (p.Phe651Ser) rs144641461 0.00011
NM_001033855.3(DCLRE1C):c.1078C>T (p.Arg360Trp) rs748164114 0.00006
NM_001033855.3(DCLRE1C):c.526A>G (p.Ile176Val) rs182977883 0.00006
NM_001033855.3(DCLRE1C):c.1865C>T (p.Thr622Ile) rs759929745 0.00004
NM_001033855.3(DCLRE1C):c.265A>G (p.Thr89Ala) rs756366535 0.00004
NM_001033855.3(DCLRE1C):c.1710T>C (p.Ile570=) rs147993236 0.00003
NM_001033855.3(DCLRE1C):c.737C>T (p.Thr246Ile) rs374596045 0.00003
NM_001033855.3(DCLRE1C):c.1288A>G (p.Arg430Gly) rs1459486949 0.00002
NM_001033855.3(DCLRE1C):c.1333C>T (p.Arg445Cys) rs774273800 0.00002
NM_001033855.3(DCLRE1C):c.350C>T (p.Pro117Leu) rs757316102 0.00002
NM_001033855.3(DCLRE1C):c.1739C>T (p.Pro580Leu) rs780103215 0.00001
NM_001033855.3(DCLRE1C):c.1964C>T (p.Ser655Leu) rs775156782 0.00001
NM_001033855.3(DCLRE1C):c.475A>T (p.Ile159Phe) rs757929355 0.00001
NM_001033855.3(DCLRE1C):c.1342A>G (p.Asn448Asp) rs483352702
NM_001033855.3(DCLRE1C):c.1379AAG[2] (p.Glu462del) rs373709012
NM_001033855.3(DCLRE1C):c.1662A>G (p.Gln554=) rs886043100
NM_001033855.3(DCLRE1C):c.1732T>C (p.Tyr578His)
NM_001033855.3(DCLRE1C):c.1903dup (p.Ser635fs) rs760288938
NM_001033855.3(DCLRE1C):c.310G>A (p.Glu104Lys)

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