ClinVar Miner

List of variants in gene NLRC5 reported as not provided by Human Evolutionary Genetics, Institut Pasteur

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Gene type:
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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_001384950.1(NLRC5):c.424+238C>T rs199475970 0.00165
NM_001384950.1(NLRC5):c.356-122C>T rs199475967 0.00161
NM_001384950.1(NLRC5):c.3920+20C>T rs199476001 0.00153
NM_001384950.1(NLRC5):c.4920-60G>A rs199476014 0.00125
NM_001384950.1(NLRC5):c.*3G>A rs199476023 0.00117
NM_001384950.1(NLRC5):c.3506+7C>T rs199475995 0.00106
NM_001384950.1(NLRC5):c.5321+11G>A rs199476020 0.00087
NM_001384950.1(NLRC5):c.2940-161G>A rs199475988 0.00086
NM_001384950.1(NLRC5):c.-12-157T>C rs199475965 0.00070
NM_001384950.1(NLRC5):c.5237+51G>A rs199476017 0.00052
NM_001330552.1(NLRC5):c.-1074G>A rs199475959 0.00042
NM_001384950.1(NLRC5):c.2418-213C>T rs199475979 0.00041
NM_001384950.1(NLRC5):c.2075+154T>C rs199475977 0.00033
NM_001384950.1(NLRC5):c.3506+149T>C rs199475996 0.00020
NM_001384950.1(NLRC5):c.*245C>T rs199476024 0.00019
NM_001384950.1(NLRC5):c.3339-404C>T rs199475994 0.00019
NM_001384950.1(NLRC5):c.5405+140G>A rs199476021 0.00019
NM_001384950.1(NLRC5):c.3203+100G>C rs199475990 0.00016
NM_001384950.1(NLRC5):c.5238-50C>T rs199476018 0.00015
NM_001384950.1(NLRC5):c.4407-9C>A rs199476008 0.00012
NM_001384950.1(NLRC5):c.2477+34T>C rs199475981 0.00010
NM_001384950.1(NLRC5):c.4919+131G>A rs199476013 0.00010
NC_000016.10:g.56989465C>G rs199475964 0.00008
NM_001384950.1(NLRC5):c.4584-134G>A rs199476010 0.00007
NM_001384950.1(NLRC5):c.3338+50C>T rs199475992 0.00006
NM_001384950.1(NLRC5):c.*285C>T rs199476025 0.00004
NM_001384950.1(NLRC5):c.2712-34C>T rs199475984 0.00004
NM_001384950.1(NLRC5):c.3506+168G>A rs199475997 0.00003
NM_001384950.1(NLRC5):c.3507-51C>T rs199475998 0.00003
NM_001384950.1(NLRC5):c.4322+98A>G rs199476006 0.00003
NM_001384950.1(NLRC5):c.5474G>A (p.Ser1825Asn) rs199476022 0.00002
NM_001384950.1(NLRC5):c.2075+113A>G rs199475976 0.00001
NM_001384950.1(NLRC5):c.2947C>G (p.His983Asp) rs199475989 0.00001
NM_001384950.1(NLRC5):c.3338+59G>A rs199475993 0.00001
NM_001384950.1(NLRC5):c.3905G>A (p.Arg1302Gln) rs199476000 0.00001
NM_001384950.1(NLRC5):c.424+276C>T rs199475971 0.00001
NM_001384950.1(NLRC5):c.424+46C>G rs199475969 0.00001
NM_001384950.1(NLRC5):c.4365C>T (p.Val1455=) rs199476007 0.00001
NM_001384950.1(NLRC5):c.4835+61C>A rs199476012 0.00001
NM_001384950.1(NLRC5):c.5172G>A (p.Ala1724=) rs199476016 0.00001
NC_000016.10:g.56989205C>T rs199475962
NM_001330552.1(NLRC5):c.-1063G>A rs199475960
NM_001330552.1(NLRC5):c.-483G>A rs199475963
NM_001330552.1(NLRC5):c.-796C>G rs199475961
NM_001384950.1(NLRC5):c.1625C>A (p.Thr542Asn) rs199475974
NM_001384950.1(NLRC5):c.2009A>C (p.Asp670Ala) rs199475975
NM_001384950.1(NLRC5):c.2076-29C>T rs199475978
NM_001384950.1(NLRC5):c.2418-199T>A rs199475980
NM_001384950.1(NLRC5):c.2477+55C>G rs199475982
NM_001384950.1(NLRC5):c.2712-121G>C rs199475983
NM_001384950.1(NLRC5):c.2754G>A (p.Val918=) rs199475985
NM_001384950.1(NLRC5):c.2870+353T>C rs199475986
NM_001384950.1(NLRC5):c.2871-27A>C rs199475987
NM_001384950.1(NLRC5):c.296-29A>C rs199475966
NM_001384950.1(NLRC5):c.3248+56T>A rs199475991
NM_001384950.1(NLRC5):c.356-88G>A rs199475968
NM_001384950.1(NLRC5):c.3596+42T>A rs199475999
NM_001384950.1(NLRC5):c.3987-248C>T rs199476002
NM_001384950.1(NLRC5):c.4500-121G>A rs199476009
NM_001384950.1(NLRC5):c.4752-73G>A rs199476011
NM_001384950.1(NLRC5):c.5004-59G>C rs199476015
NM_001384950.1(NLRC5):c.5251A>G (p.Lys1751Glu) rs199476019
NM_001384950.1(NLRC5):c.847A>G (p.Ser283Gly) rs199475972
NM_001384950.1(NLRC5):c.856T>G (p.Ser286Ala) rs1555520385

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