ClinVar Miner

List of variants in gene ARID1A reported by Genetic Services Laboratory, University of Chicago

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Gene type:
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Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_006015.6(ARID1A):c.5114A>G (p.Asn1705Ser) rs61756316 0.00698
NM_006015.6(ARID1A):c.358C>T (p.Pro120Ser) rs571264557 0.00572
NM_006015.6(ARID1A):c.6586C>T (p.Leu2196=) rs149633292 0.00468
NM_006015.6(ARID1A):c.5001G>A (p.Pro1667=) rs116540923 0.00363
NM_006015.6(ARID1A):c.2541C>A (p.Ile847=) rs151274586 0.00329
NM_006015.6(ARID1A):c.318C>T (p.Asn106=) rs551186176 0.00196
NM_006015.6(ARID1A):c.135C>T (p.Ala45=) rs892415319 0.00168
NM_006015.6(ARID1A):c.5779G>C (p.Ala1927Pro) rs143257313 0.00131
NM_006015.6(ARID1A):c.5336A>G (p.Glu1779Gly) rs140946580 0.00112
NM_006015.6(ARID1A):c.472C>T (p.Pro158Ser) rs567246585 0.00088
NM_006015.6(ARID1A):c.162C>T (p.Ala54=) rs1001634270 0.00068
NM_006015.6(ARID1A):c.3762C>T (p.Gly1254=) rs138814830 0.00060
NM_006015.6(ARID1A):c.4560C>T (p.Gly1520=) rs138023869 0.00041
NM_006015.6(ARID1A):c.5076C>T (p.Asn1692=) rs149468118 0.00038
NM_006015.6(ARID1A):c.4779G>T (p.Arg1593=) rs140978841 0.00033
NM_006015.6(ARID1A):c.4053C>T (p.Gly1351=) rs200122106 0.00031
NM_006015.6(ARID1A):c.6659A>G (p.Asn2220Ser) rs139576809 0.00029
NM_006015.6(ARID1A):c.1803+9T>C rs371726505 0.00025
NM_006015.6(ARID1A):c.2139A>G (p.Pro713=) rs779283100 0.00023
NM_006015.6(ARID1A):c.5491C>G (p.Leu1831Val) rs150534917 0.00022
NM_006015.6(ARID1A):c.2698G>A (p.Ala900Thr) rs138418893 0.00019
NM_006015.6(ARID1A):c.-7G>T rs1421881390 0.00018
NM_006015.6(ARID1A):c.110G>A (p.Gly37Asp) rs933617964 0.00014
NM_006015.6(ARID1A):c.2204G>A (p.Ser735Asn) rs142353005 0.00011
NM_006015.6(ARID1A):c.3978G>A (p.Pro1326=) rs370696498 0.00008
NM_006015.6(ARID1A):c.6252C>G (p.Val2084=) rs145004598 0.00008
NM_006015.6(ARID1A):c.268A>G (p.Ser90Gly) rs752026201 0.00007
NM_006015.6(ARID1A):c.3816G>A (p.Ala1272=) rs763151089 0.00007
NM_006015.6(ARID1A):c.2123A>C (p.Gln708Pro) rs367889013 0.00006
NM_006015.6(ARID1A):c.1329C>T (p.Gly443=) rs369923774 0.00005
NM_006015.6(ARID1A):c.550C>T (p.Leu184=) rs761025553 0.00004
NM_006015.6(ARID1A):c.1619C>T (p.Thr540Met) rs892173376 0.00003
NM_006015.6(ARID1A):c.1892G>C (p.Ser631Thr) rs748512916 0.00002
NM_006015.6(ARID1A):c.4777C>T (p.Arg1593Trp) rs201556442 0.00002
NM_006015.6(ARID1A):c.6785C>T (p.Ser2262Leu) rs375849292 0.00002
NM_006015.6(ARID1A):c.2320C>T (p.Arg774Cys) rs1466882490 0.00001
NM_006015.6(ARID1A):c.2512G>A (p.Gly838Arg) rs753334968 0.00001
NM_006015.6(ARID1A):c.2818A>G (p.Met940Val) rs999287309 0.00001
NM_006015.6(ARID1A):c.2870A>G (p.Asn957Ser) rs758593161 0.00001
NM_006015.6(ARID1A):c.5305C>G (p.Leu1769Val) rs1557619767 0.00001
NM_006015.6(ARID1A):c.5442A>G (p.Val1814=) rs1413966888 0.00001
NM_006015.6(ARID1A):c.114GGC[6] (p.Ala45dup) rs587779737
NM_006015.6(ARID1A):c.1351-10T>C rs1169817343
NM_006015.6(ARID1A):c.1397del (p.Gly466fs)
NM_006015.6(ARID1A):c.1440G>A (p.Gln480=) rs746775479
NM_006015.6(ARID1A):c.239A>G (p.Asn80Ser) rs1553145891
NM_006015.6(ARID1A):c.2449G>T (p.Ala817Ser) rs1553152137
NM_006015.6(ARID1A):c.249CGG[6] (p.Gly86_Gly87dup) rs1015322780
NM_006015.6(ARID1A):c.250_267dup (p.Gly84_Gly89dup) rs777773061
NM_006015.6(ARID1A):c.264C>T (p.Ala88=) rs765913797
NM_006015.6(ARID1A):c.31_56del (p.Ser11fs) rs797045262
NM_006015.6(ARID1A):c.3234C>T (p.Thr1078=)
NM_006015.6(ARID1A):c.326C>T (p.Pro109Leu) rs1167372383
NM_006015.6(ARID1A):c.394del (p.Val132fs) rs797045263
NM_006015.6(ARID1A):c.3975C>G (p.Pro1325=) rs148038965
NM_006015.6(ARID1A):c.3978GCA[10] (p.Gln1333_Gln1334dup) rs374564889
NM_006015.6(ARID1A):c.3978GCA[9] (p.Gln1334dup) rs374564889
NM_006015.6(ARID1A):c.4123G>A (p.Gly1375Ser) rs2124117067
NM_006015.6(ARID1A):c.4472T>C (p.Val1491Ala)
NM_006015.6(ARID1A):c.483CGC[5] (p.Ala167dup) rs759913677
NM_006015.6(ARID1A):c.48GCC[6] (p.Pro21dup) rs748085214
NM_006015.6(ARID1A):c.4986A>G (p.Lys1662=) rs1553153328
NM_006015.6(ARID1A):c.5138T>C (p.Leu1713Pro) rs797045264
NM_006015.6(ARID1A):c.513ACA[1] (p.Gln172del) rs1557570075
NM_006015.6(ARID1A):c.5164C>T (p.Arg1722Ter) rs1485978447
NM_006015.6(ARID1A):c.5287GAA[4] (p.Glu1767del) rs753766136
NM_006015.6(ARID1A):c.5303T>C (p.Leu1768Pro) rs1302313826
NM_006015.6(ARID1A):c.5717G>A (p.Arg1906Gln) rs41303631
NM_006015.6(ARID1A):c.5719A>G (p.Ile1907Val) rs139230162
NM_006015.6(ARID1A):c.5745G>T (p.Leu1915Phe) rs767902770
NM_006015.6(ARID1A):c.587C>T (p.Ala196Val) rs1352086990
NM_006015.6(ARID1A):c.6169C>T (p.Arg2057Trp)
NM_006015.6(ARID1A):c.6518A>G (p.Asn2173Ser) rs1553153783
NM_006015.6(ARID1A):c.6544G>C (p.Ala2182Pro) rs1553153787

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