ClinVar Miner

List of variants in gene IFT172 reported as pathogenic by Invitae

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_015662.3(IFT172):c.112C>T (p.Arg38Ter) rs139021548 0.00004
NM_015662.3(IFT172):c.1525-1G>A rs370540673 0.00001
NM_015662.3(IFT172):c.2365C>T (p.Arg789Ter) rs202024173 0.00001
NM_015662.3(IFT172):c.2866C>T (p.Gln956Ter) rs144450109 0.00001
NM_015662.3(IFT172):c.4508G>A (p.Trp1503Ter) rs1665288663 0.00001
NM_015662.3(IFT172):c.4519C>T (p.Arg1507Ter) rs150246251 0.00001
NM_015662.3(IFT172):c.4597dup (p.Thr1533fs) rs1183354903 0.00001
NC_000002.11:g.(?_27693775)_(27695249_?)del
NC_000002.12:g.(?_27462701)_(27463181_?)del
NM_015662.3(IFT172):c.1036C>T (p.Arg346Ter) rs201862538
NM_015662.3(IFT172):c.1078del (p.Glu359_Val360insTer) rs1453282096
NM_015662.3(IFT172):c.1100_1103dup (p.Tyr368Ter)
NM_015662.3(IFT172):c.1115dup (p.His372fs) rs2148544061
NM_015662.3(IFT172):c.1209del (p.Phe403fs) rs2148542989
NM_015662.3(IFT172):c.1315dup (p.His439fs)
NM_015662.3(IFT172):c.1412-1G>C
NM_015662.3(IFT172):c.1412-2A>G
NM_015662.3(IFT172):c.148A>T (p.Arg50Ter) rs1668686361
NM_015662.3(IFT172):c.1555A>T (p.Lys519Ter)
NM_015662.3(IFT172):c.1671_1672dup (p.Val558fs) rs587777083
NM_015662.3(IFT172):c.1871_1872del (p.Thr624fs)
NM_015662.3(IFT172):c.189_192del (p.Lys65fs)
NM_015662.3(IFT172):c.1972C>T (p.Arg658Ter)
NM_015662.3(IFT172):c.2078del (p.Lys693fs) rs1444591972
NM_015662.3(IFT172):c.2146C>T (p.Gln716Ter) rs2148507566
NM_015662.3(IFT172):c.2158del (p.Arg720fs) rs587777086
NM_015662.3(IFT172):c.2209G>T (p.Glu737Ter)
NM_015662.3(IFT172):c.2224_2236dup (p.Trp746Ter)
NM_015662.3(IFT172):c.2233C>T (p.Gln745Ter)
NM_015662.3(IFT172):c.3130C>T (p.Arg1044Ter)
NM_015662.3(IFT172):c.3426del (p.Glu1143fs)
NM_015662.3(IFT172):c.4194dup (p.Phe1399fs) rs2148477695
NM_015662.3(IFT172):c.4493_4494del (p.Glu1498fs)
NM_015662.3(IFT172):c.455_462dup (p.Val155fs)
NM_015662.3(IFT172):c.4642C>T (p.Gln1548Ter)
NM_015662.3(IFT172):c.691del (p.Thr231fs)
NM_015662.3(IFT172):c.811C>T (p.Arg271Ter) rs1250676888
NM_015662.3(IFT172):c.875del (p.Leu292fs)
NM_015662.3(IFT172):c.952C>T (p.Arg318Ter)
NM_015662.3(IFT172):c.978dup (p.Glu327Ter)

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