ClinVar Miner

List of variants reported as pathogenic for ciliopathy by Molecular Genetics Laboratory, Institute for Ophthalmic Research

Included ClinVar conditions (273):
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Minimum conflict level:
ClinVar version:
Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_152618.3(BBS12):c.1237C>G (p.Leu413Val) rs758217005 0.00012
NM_001278293.3(ARL6):c.291T>A (p.Ser97Arg) rs2037381055 0.00001
NM_033028.5(BBS4):c.883C>T (p.Arg295Ter) rs775710800 0.00001
NM_152618.3(BBS12):c.1504G>T (p.Ala502Ser) rs142593414 0.00001
NM_001278293.3(ARL6):c.528G>T (p.Trp176Cys) rs2037751886
NM_001378454.1(ALMS1):c.10146dup (p.Ser3383fs) rs1553416872
NM_001378454.1(ALMS1):c.7132C>T (p.Leu2378Phe) rs768751472
NM_001378454.1(ALMS1):c.7786C>T (p.Gln2596Ter) rs1672934629
NM_024685.4(BBS10):c.1603_1606del (p.Asp535fs) rs1951757988
NM_024685.4(BBS10):c.578T>C (p.Leu193Ser) rs1951767864
NM_033028.5(BBS4):c.129T>G (p.Tyr43Ter) rs2065331681

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