ClinVar Miner

List of variants in gene NFATC1 reported as benign for not provided

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Gene type:
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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_001278669.2(NFATC1):c.1986A>G (p.Pro662=) rs25656 0.40597
NM_001278669.2(NFATC1):c.1851T>C (p.Ser617=) rs15350 0.23398
NM_001278669.2(NFATC1):c.1226+17G>A rs113881412 0.10427
NM_001278669.2(NFATC1):c.202C>A (p.Pro68Thr) rs1051978 0.07673
NM_001278669.2(NFATC1):c.1527C>T (p.Ala509=) rs25657 0.07317
NM_001278669.2(NFATC1):c.2280G>A (p.Ala760=) rs1063671 0.04597
NM_001278669.2(NFATC1):c.1983G>A (p.Pro661=) rs25658 0.03875
NM_001278669.2(NFATC1):c.267C>T (p.Tyr89=) rs55863211 0.02690
NM_001278669.2(NFATC1):c.291C>T (p.Pro97=) rs1063668 0.02399
NM_001278669.2(NFATC1):c.855G>A (p.Pro285=) rs1063670 0.01722
NM_001278669.2(NFATC1):c.294G>A (p.Ala98=) rs2230113 0.01244
NM_001278669.2(NFATC1):c.2064C>T (p.Tyr688=) rs35099556 0.01104
NM_001278669.2(NFATC1):c.153C>T (p.Asn51=) rs150374931 0.00997
NM_001278669.2(NFATC1):c.204G>A (p.Pro68=) rs138101748 0.00587
NM_001278669.2(NFATC1):c.105C>T (p.Gly35=) rs374280400 0.00528
NM_001278669.2(NFATC1):c.2372C>T (p.Pro791Leu) rs200207441 0.00387
NM_001278669.2(NFATC1):c.237C>T (p.Ile79=) rs149452763 0.00387
NM_001278669.2(NFATC1):c.723G>A (p.Ser241=) rs61731548 0.00368
NM_001278669.2(NFATC1):c.2383G>A (p.Gly795Arg) rs56191735 0.00303
NM_001278669.2(NFATC1):c.1446C>T (p.Asp482=) rs146371354 0.00264
NM_001278669.2(NFATC1):c.1589+8G>A rs201427841 0.00199
NM_001278669.2(NFATC1):c.1056C>T (p.Pro352=) rs139217071 0.00188
NM_001278669.2(NFATC1):c.1239C>T (p.Pro413=) rs139104184 0.00172
NM_001278669.2(NFATC1):c.1069C>G (p.Leu357Val) rs143975184 0.00165
NM_001278669.2(NFATC1):c.2239G>A (p.Gly747Ser) rs139715685 0.00086
NM_001278669.2(NFATC1):c.567C>T (p.Tyr189=) rs140225213 0.00080
NM_001278669.2(NFATC1):c.1461C>T (p.Arg487=) rs144047751 0.00062
NM_001278669.2(NFATC1):c.1326C>T (p.Tyr442=) rs75223694 0.00058
NM_001278669.2(NFATC1):c.1521C>T (p.His507=) rs200262117 0.00019
NM_001278669.2(NFATC1):c.2337C>T (p.Gly779=) rs143214085 0.00017
NM_001278669.2(NFATC1):c.2364C>T (p.Leu788=) rs771802842 0.00009
NM_001278669.2(NFATC1):c.636C>G (p.Pro212=) rs577582640 0.00009
NM_001278669.2(NFATC1):c.104G>A (p.Gly35Asp) rs200585424
NM_001278669.2(NFATC1):c.1104C>T (p.Pro368=) rs143180395
NM_001278669.2(NFATC1):c.2251T>G (p.Cys751Gly) rs754093
NM_001278669.2(NFATC1):c.2289C>T (p.Gly763=) rs7233684
NM_001278669.2(NFATC1):c.2290G>A (p.Val764Met) rs145230460
NM_001278669.2(NFATC1):c.786T>G (p.Pro262=) rs2230112

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