ClinVar Miner

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

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Total variants: 36
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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.135C>T (p.Ala45=) rs892415319 0.00168
NM_006015.6(ARID1A):c.162C>T (p.Ala54=) rs1001634270 0.00068
NM_006015.6(ARID1A):c.4560C>T (p.Gly1520=) rs138023869 0.00041
NM_006015.6(ARID1A):c.4779G>T (p.Arg1593=) rs140978841 0.00033
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.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.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.2818A>G (p.Met940Val) rs999287309 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.250_267dup (p.Gly84_Gly89dup) rs777773061
NM_006015.6(ARID1A):c.264C>T (p.Ala88=) rs765913797
NM_006015.6(ARID1A):c.3234C>T (p.Thr1078=)
NM_006015.6(ARID1A):c.326C>T (p.Pro109Leu) rs1167372383
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.48GCC[6] (p.Pro21dup) rs748085214
NM_006015.6(ARID1A):c.4986A>G (p.Lys1662=) rs1553153328
NM_006015.6(ARID1A):c.513ACA[1] (p.Gln172del) rs1557570075
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.5719A>G (p.Ile1907Val) rs139230162

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