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"ClinicalSignificance": "Uncertain", "RCVaccession": "RCV000417205", "dbSNP": "193922737", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 564, "Mutation": "D564H", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV000417204", "dbSNP": "193922736", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 561, "Mutation": "P561L", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV000417199", "dbSNP": "193922735", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 560, "Mutation": "E560G", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV000417202", "dbSNP": "193922734", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 1204, "Mutation": "R1204C", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000279946|RCV000883389", "dbSNP": "56116165", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 1175, "Mutation": "I1175V", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV000352617", "dbSNP": "761259011", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 1173, "Mutation": "P1173Q", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000293015", "dbSNP": "117902541", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 891, "Mutation": "T891M", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000354003|RCV000971123", "dbSNP": "56081375", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 790, "Mutation": "T790N", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000311885|RCV000953043", "dbSNP": "56227191", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 630, "Mutation": "S630P", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000290625|RCV002522971", "dbSNP": "56030257", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 16, "Mutation": "T16I", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000338395|RCV002522966", "dbSNP": "61754325", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 1084, "Mutation": "V1084A", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000387384|RCV000912774", "dbSNP": "148648427", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 961, "Mutation": "P961S", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000327309|RCV001528080", "dbSNP": "2290041", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 863, "Mutation": "L863R", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000301297", "dbSNP": "545588214", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 738, "Mutation": "R738Q", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000351244|RCV002521109", "dbSNP": "200823152", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 610, "Mutation": "S610F", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003293286", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 786, "Mutation": "L786P", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003261881", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 457, "Mutation": "L457Q", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003287050", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 164, "Mutation": "A164V", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003286885", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 487, "Mutation": "E487K", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003242114", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 414, "Mutation": "R414P", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003270480", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 947, "Mutation": "G947R", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003259739", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 22, "Mutation": "L22V", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003211873", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 968, "Mutation": "P968A", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003199870", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 808, "Mutation": "G808R", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003209453", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 165, "Mutation": "V165L", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003210374", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 443, "Mutation": "A443V", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003192762", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 891, "Mutation": "T891A", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003189501", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1081, "Mutation": "G1081E", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003139361", "dbSNP": "", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 178, "Mutation": "I178T", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002748914", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 969, "Mutation": "V969I", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002980016", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1158, "Mutation": "K1158N", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002947096", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 35, "Mutation": "R35C", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002959886", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1094, "Mutation": "P1094R", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002944556", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 47, "Mutation": "S47F", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002925080", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 672, "Mutation": "P672T", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002940873", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 567, "Mutation": "Q567R", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002897375", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 887, "Mutation": "T887A", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002901116", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1016, "Mutation": "R1016C", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002900724", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 962, "Mutation": "S962T", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002869302", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 719, "Mutation": "M719V", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002896848", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 464, "Mutation": "R464P", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002869586", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 326, "Mutation": "T326K", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002845370", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 916, "Mutation": "P916S", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002844924", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 295, "Mutation": "V295G", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002840374", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 52, "Mutation": "P52A", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002798534", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 314, "Mutation": "T314I", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002808685", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 558, "Mutation": "P558S", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002797979", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1140, "Mutation": "S1140C", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002772417", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 301, "Mutation": "R301G", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002757861", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 345, "Mutation": "P345S", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002787465", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 6, "Mutation": "A6D", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002712753", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 217, "Mutation": "R217H", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002691692", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 50, "Mutation": "A50T", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002677926", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 699, "Mutation": "K699E", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003054612", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 184, "Mutation": "S184P", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003025194", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 125, "Mutation": "P125R", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002929213", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 61, "Mutation": "R61H", "Disease": "-", "ClinicalSignificance": "Benign", "RCVaccession": "RCV002953435", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1198, "Mutation": "R1198H", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002943428|RCV003226561", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1231, "Mutation": "S1231R", "Disease": "-", "ClinicalSignificance": "Benign", "RCVaccession": "RCV002967506", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 843, "Mutation": "F843L", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002948752", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 639, "Mutation": "G639R", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002933822|RCV002957182", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 669, "Mutation": "R669Q", "Disease": "-", "ClinicalSignificance": "Benign", "RCVaccession": "RCV002937604", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1063, "Mutation": "G1063R", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002928526|RCV002928527", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 965, "Mutation": "L965F", "Disease": "-", "ClinicalSignificance": "Benign", "RCVaccession": "RCV002909891", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 608, "Mutation": "V608M", "Disease": "-", "ClinicalSignificance": "Benign", "RCVaccession": "RCV002923266", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 846, "Mutation": "I846V", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002900416", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 12, "Mutation": "L12R", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002861476", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 556, "Mutation": "P556A", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002781403", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1187, "Mutation": "R1187C", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002781457|RCV002795325", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 231, "Mutation": "P231L", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002770980", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 608, "Mutation": "V608L", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002765412", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 436, "Mutation": "R436S", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002717275|RCV002730155", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 196, "Mutation": "T196N", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002734952", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 416, "Mutation": "D416Y", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002663474", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 486, "Mutation": "E486K", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002627000", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1184, "Mutation": "S1184G", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002630395", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 235, "Mutation": "R235C", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003118017", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 90, "Mutation": "A90S", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003105011", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 511, "Mutation": "R511C", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002638568|RCV002654899", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 159, "Mutation": "D159G", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002619463", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 244, "Mutation": "L244P", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002627796", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1061, "Mutation": "G1061A", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003078738|RCV003089664|RCV003151441", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 98, "Mutation": "P98T", "Disease": "-", "ClinicalSignificance": "Benign", "RCVaccession": "RCV003089342", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1168, "Mutation": "G1168E", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV003064446", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 753, "Mutation": "G753D", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV002292005", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 169, "Mutation": "P169L", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Pathogenic", "RCVaccession": "RCV001849665", "dbSNP": "", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 525, "Mutation": "R525G", "Disease": "-", "ClinicalSignificance": "Benign", "RCVaccession": "RCV001445335", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 259, "Mutation": "S259L", "Disease": "-", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV001356333", "dbSNP": "", "MIMID": "nan"}, {"protein_id": "WNK4-201", "Position": 1199, "Mutation": "R1199C", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV001127473|RCV002556787", "dbSNP": "200519604", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 1147, "Mutation": "S1147L", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV001127472", "dbSNP": "768159533", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 1137, "Mutation": "E1137K", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV001125385", "dbSNP": "773000314", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 1075, "Mutation": "R1075C", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV001125384", "dbSNP": "201421543", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 1011, "Mutation": "P1011L", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV001125383", "dbSNP": "61755628", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 954, "Mutation": "P954S", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV001124390", "dbSNP": "2054652994", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 894, "Mutation": "P894L", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV001124388", "dbSNP": "2054650116", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 783, "Mutation": "N783S", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV001123283", "dbSNP": "145613797", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 766, "Mutation": "E766G", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV001127355", "dbSNP": "778394259", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 755, "Mutation": "M755K", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV001127354", "dbSNP": "2054629400", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 677, "Mutation": "R677Q", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV001127353", "dbSNP": "772583212", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 736, "Mutation": "R736Q", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000289222", "dbSNP": "149389156", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 669, "Mutation": "R669W", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Uncertain", "RCVaccession": "RCV000402811|RCV002522972|RCV003243078", "dbSNP": "769815091", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 618, "Mutation": "C618F", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000286594|RCV002522970", "dbSNP": "143396070", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 601, "Mutation": "A601S", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000259612|RCV001723910", "dbSNP": "55781437", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 80, "Mutation": "A80D", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000371996|RCV000957610", "dbSNP": "61754326", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 6, "Mutation": "A6T", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000281170|RCV000971310", "dbSNP": "61754324", "MIMID": "614491"}, {"protein_id": "WNK4-201", "Position": 1025, "Mutation": "P1025L", "Disease": "Pseudohypoaldosteronism, Type IIB", "ClinicalSignificance": "Benign", "RCVaccession": "RCV000328268|RCV000948453", "dbSNP": "56099549", 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