ClinVar Miner

List of variants in gene ARID1B reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 98
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HGVS dbSNP gnomAD frequency
NM_001374828.1(ARID1B):c.3235+6C>T rs148976215 0.00384
NM_001374828.1(ARID1B):c.3768C>T (p.Thr1256=) rs142391292 0.00312
NM_001374828.1(ARID1B):c.2187C>T (p.Pro729=) rs146240413 0.00310
NM_001374828.1(ARID1B):c.1194A>C (p.Gly398=) rs112474841 0.00209
NM_001374828.1(ARID1B):c.2286G>A (p.Thr762=) rs6912981 0.00191
NM_001374828.1(ARID1B):c.3681C>T (p.Tyr1227=) rs61736269 0.00189
NM_001374828.1(ARID1B):c.963C>T (p.Ala321=) rs533517668 0.00107
NM_001374828.1(ARID1B):c.3105C>T (p.Pro1035=) rs144894118 0.00106
NM_001374828.1(ARID1B):c.5384A>G (p.Asn1795Ser) rs140177120 0.00079
NM_001374828.1(ARID1B):c.2548G>A (p.Ala850Thr) rs147784000 0.00071
NM_001374828.1(ARID1B):c.1280C>T (p.Ala427Val) rs530780611 0.00068
NM_001374828.1(ARID1B):c.3072G>C (p.Ala1024=) rs148749268 0.00067
NM_001374828.1(ARID1B):c.1191C>A (p.Gly397=) rs184815562 0.00064
NM_001374828.1(ARID1B):c.1771C>T (p.Pro591Ser) rs200682868 0.00062
NM_001374828.1(ARID1B):c.2815G>A (p.Gly939Ser) rs145635490 0.00046
NM_001374828.1(ARID1B):c.3188A>T (p.Gln1063Leu) rs139620600 0.00038
NM_001374828.1(ARID1B):c.4315G>A (p.Gly1439Arg) rs199674889 0.00026
NM_001374828.1(ARID1B):c.7023C>T (p.His2341=) rs183572405 0.00023
NM_001374828.1(ARID1B):c.5679C>T (p.Ala1893=) rs146982427 0.00021
NM_001374828.1(ARID1B):c.6318C>T (p.His2106=) rs142416998 0.00017
NM_001374828.1(ARID1B):c.2319C>T (p.Ser773=) rs148700132 0.00016
NM_001374828.1(ARID1B):c.4603T>G (p.Ser1535Ala) rs145516400 0.00016
NM_001374828.1(ARID1B):c.5544A>C (p.Ala1848=) rs148922487 0.00014
NM_001374828.1(ARID1B):c.5601C>T (p.Asp1867=) rs368980689 0.00014
NM_001374828.1(ARID1B):c.5678C>T (p.Ala1893Val) rs201137071 0.00014
NM_001374828.1(ARID1B):c.1881G>A (p.Pro627=) rs142939952 0.00013
NM_001374828.1(ARID1B):c.6450G>A (p.Thr2150=) rs753595827 0.00013
NM_001374828.1(ARID1B):c.1928T>C (p.Ile643Thr) rs756050584 0.00011
NM_001374828.1(ARID1B):c.1337C>T (p.Ala446Val) rs748273011 0.00008
NM_001374828.1(ARID1B):c.1841T>C (p.Met614Thr) rs141260832 0.00008
NM_001374828.1(ARID1B):c.2280G>A (p.Thr760=) rs201290874 0.00006
NM_001374828.1(ARID1B):c.2736A>G (p.Pro912=) rs368988882 0.00006
NM_001374828.1(ARID1B):c.5640C>T (p.Ser1880=) rs555132244 0.00006
NM_001374828.1(ARID1B):c.4509C>T (p.Tyr1503=) rs377021700 0.00004
NM_001374828.1(ARID1B):c.5040G>A (p.Ala1680=) rs374125873 0.00003
NM_001374828.1(ARID1B):c.1962C>T (p.Ala654=) rs752755002 0.00002
NM_001374828.1(ARID1B):c.5096C>T (p.Pro1699Leu) rs1455506883 0.00002
NM_001374828.1(ARID1B):c.5903G>A (p.Arg1968His) rs374035954 0.00002
NM_001374828.1(ARID1B):c.2430T>A (p.Val810=) rs766684321 0.00001
NM_001374828.1(ARID1B):c.3588C>T (p.Val1196=) rs371828409 0.00001
NM_001374828.1(ARID1B):c.4370G>A (p.Ser1457Asn) rs142808724 0.00001
NM_001374828.1(ARID1B):c.4611G>A (p.Pro1537=) rs749608995 0.00001
NM_001374828.1(ARID1B):c.5148C>T (p.Thr1716=) rs745670548 0.00001
NM_001374828.1(ARID1B):c.6172G>A (p.Ala2058Thr) rs772464386 0.00001
NM_001374828.1(ARID1B):c.1058CCG[6] (p.Ala357dup) rs766956053
NM_001374828.1(ARID1B):c.1170CGG[10] (p.Gly401_Gly402dup) rs587779747
NM_001374828.1(ARID1B):c.1170CGG[3] (p.Gly398_Gly402del) rs587779747
NM_001374828.1(ARID1B):c.1170CGG[4] (p.Gly399_Gly402del) rs587779747
NM_001374828.1(ARID1B):c.1211GAG[5] (p.Gly409_Gly411del) rs747790383
NM_001374828.1(ARID1B):c.1211GAG[6] (p.Gly410_Gly411del) rs747790383
NM_001374828.1(ARID1B):c.1211GAG[9] (p.Gly411dup) rs747790383
NM_001374828.1(ARID1B):c.1221A>C (p.Gly407=)
NM_001374828.1(ARID1B):c.1238GAGCAGGAG[1] (p.413GAG[1]) rs771557031
NM_001374828.1(ARID1B):c.1247G>C (p.Gly416Ala)
NM_001374828.1(ARID1B):c.1265_1270dup (p.Val422_Ala423dup) rs759630370
NM_001374828.1(ARID1B):c.1278C>G (p.Ala426=)
NM_001374828.1(ARID1B):c.1278_1286del (p.Ala431_Ala433del)
NM_001374828.1(ARID1B):c.1292CAG[4] (p.Ala433dup) rs797045267
NM_001374828.1(ARID1B):c.1303GGC[4] (p.Gly439_Gly440del) rs797045268
NM_001374828.1(ARID1B):c.1303GGC[7] (p.Gly440dup) rs797045268
NM_001374828.1(ARID1B):c.1341G>A (p.Gly447=)
NM_001374828.1(ARID1B):c.1360C>G (p.Pro454Ala) rs1778962227
NM_001374828.1(ARID1B):c.1436G>C (p.Gly479Ala) rs760718156
NM_001374828.1(ARID1B):c.1608C>A (p.Pro536=)
NM_001374828.1(ARID1B):c.1676G>C (p.Gly559Ala)
NM_001374828.1(ARID1B):c.1739G>A (p.Ser580Asn)
NM_001374828.1(ARID1B):c.1764C>T (p.Thr588=) rs1317584691
NM_001374828.1(ARID1B):c.1776C>G (p.Thr592=)
NM_001374828.1(ARID1B):c.1987-29739A>G
NM_001374828.1(ARID1B):c.2072C>T (p.Pro691Leu)
NM_001374828.1(ARID1B):c.2655G>A (p.Ser885=)
NM_001374828.1(ARID1B):c.3210G>A (p.Ala1070=)
NM_001374828.1(ARID1B):c.3330C>T (p.Pro1110=) rs752231248
NM_001374828.1(ARID1B):c.3645C>T (p.Ala1215=)
NM_001374828.1(ARID1B):c.3678C>G (p.Leu1226=) rs111368751
NM_001374828.1(ARID1B):c.3682G>A (p.Val1228Ile)
NM_001374828.1(ARID1B):c.3909G>A (p.Pro1303=)
NM_001374828.1(ARID1B):c.3919+2029G>A
NM_001374828.1(ARID1B):c.3919+2101G>A
NM_001374828.1(ARID1B):c.4613A>G (p.Asp1538Gly)
NM_001374828.1(ARID1B):c.4641G>A (p.Pro1547=)
NM_001374828.1(ARID1B):c.5126C>T (p.Thr1709Met)
NM_001374828.1(ARID1B):c.5310T>C (p.Leu1770=) rs372621575
NM_001374828.1(ARID1B):c.5409C>T (p.Leu1803=)
NM_001374828.1(ARID1B):c.5442G>C (p.Leu1814=) rs754864354
NM_001374828.1(ARID1B):c.5626G>A (p.Glu1876Lys)
NM_001374828.1(ARID1B):c.5649G>A (p.Lys1883=)
NM_001374828.1(ARID1B):c.5694G>A (p.Lys1898=)
NM_001374828.1(ARID1B):c.5769T>A (p.Val1923=)
NM_001374828.1(ARID1B):c.6021G>T (p.Arg2007=) rs770037041
NM_001374828.1(ARID1B):c.6042C>T (p.Asp2014=)
NM_001374828.1(ARID1B):c.6043G>A (p.Ala2015Thr)
NM_001374828.1(ARID1B):c.6465C>T (p.Ser2155=)
NM_001374828.1(ARID1B):c.6546G>A (p.Pro2182=)
NM_001374828.1(ARID1B):c.6546G>C (p.Pro2182=)
NM_001374828.1(ARID1B):c.6795C>T (p.Asp2265=)
NM_001374828.1(ARID1B):c.6996C>T (p.Asp2332=)
NM_001374828.1(ARID1B):c.954C>T (p.Gly318=) rs745740327

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