ClinVar Miner

Variants in gene ARID1A with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 80
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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.6586C>T (p.Leu2196=) rs149633292 0.00468
NM_006015.6(ARID1A):c.1188C>T (p.Gly396=) rs61749356 0.00330
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 0.00162
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.4869G>A (p.Ser1623=) rs148936933 0.00106
NM_006015.6(ARID1A):c.4152C>T (p.His1384=) rs149908828 0.00100
NM_006015.6(ARID1A):c.472C>T (p.Pro158Ser) rs567246585 0.00088
NM_006015.6(ARID1A):c.2123A>C (p.Gln708Pro) rs367889013 0.00086
NM_006015.6(ARID1A):c.373G>A (p.Gly125Ser) rs536658556 0.00071
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.3792C>T (p.Ala1264=) rs142429183 0.00059
NM_006015.6(ARID1A):c.4563C>T (p.Pro1521=) rs149095176 0.00058
NM_006015.6(ARID1A):c.1716G>A (p.Thr572=) rs147554664 0.00055
NM_006015.6(ARID1A):c.1266C>T (p.Tyr422=) rs144272459 0.00039
NM_006015.6(ARID1A):c.3242A>G (p.Asn1081Ser) rs148400981 0.00039
NM_006015.6(ARID1A):c.4560C>T (p.Gly1520=) rs138023869 0.00039
NM_006015.6(ARID1A):c.5076C>T (p.Asn1692=) rs149468118 0.00037
NM_006015.6(ARID1A):c.4779G>T (p.Arg1593=) rs140978841 0.00033
NM_006015.6(ARID1A):c.2074A>G (p.Ile692Val) rs146402512 0.00032
NM_006015.6(ARID1A):c.4879C>G (p.Pro1627Ala) rs151074395 0.00032
NM_006015.6(ARID1A):c.4053C>T (p.Gly1351=) rs200122106 0.00031
NM_006015.6(ARID1A):c.4702C>T (p.Pro1568Ser) rs113718290 0.00030
NM_006015.6(ARID1A):c.6659A>G (p.Asn2220Ser) rs139576809 0.00029
NM_006015.6(ARID1A):c.4347C>T (p.Gly1449=) rs140481844 0.00023
NM_006015.6(ARID1A):c.2139A>G (p.Pro713=) rs779283100 0.00022
NM_006015.6(ARID1A):c.1597C>T (p.Pro533Ser) rs200572766 0.00021
NM_006015.6(ARID1A):c.2698G>A (p.Ala900Thr) rs138418893 0.00019
NM_006015.6(ARID1A):c.405T>G (p.Pro135=) rs922780561 0.00013
NM_006015.6(ARID1A):c.2298G>A (p.Gln766=) rs572510196 0.00012
NM_006015.6(ARID1A):c.4542G>A (p.Thr1514=) rs560211386 0.00012
NM_006015.6(ARID1A):c.5615C>T (p.Ala1872Val) rs191813608 0.00011
NM_006015.6(ARID1A):c.456A>G (p.Gln152=) rs1043397333 0.00010
NM_006015.6(ARID1A):c.4751A>G (p.Gln1584Arg) rs558739370 0.00008
NM_006015.6(ARID1A):c.501C>T (p.Ala167=) rs754018917 0.00008
NM_006015.6(ARID1A):c.268A>G (p.Ser90Gly) rs752026201 0.00007
NM_006015.6(ARID1A):c.3046G>A (p.Gly1016Ser) rs182858322 0.00007
NM_006015.6(ARID1A):c.3816G>A (p.Ala1272=) rs763151089 0.00007
NM_006015.6(ARID1A):c.372C>T (p.Gly124=) rs1005812119 0.00006
NM_006015.6(ARID1A):c.148A>G (p.Met50Val) rs1216784088 0.00005
NM_006015.6(ARID1A):c.3967C>T (p.Arg1323Cys) rs587778051 0.00005
NM_006015.6(ARID1A):c.3972C>T (p.Tyr1324=) rs377622327 0.00005
NM_006015.6(ARID1A):c.5311C>T (p.Pro1771Ser) rs187631645 0.00005
NM_006015.6(ARID1A):c.111C>T (p.Gly37=) rs1057522894 0.00004
NM_006015.6(ARID1A):c.4081A>G (p.Met1361Val) rs770710220 0.00004
NM_006015.6(ARID1A):c.5647A>T (p.Thr1883Ser) rs150076443 0.00004
NM_006015.6(ARID1A):c.6711G>A (p.Ala2237=) rs542602060 0.00004
NM_006015.6(ARID1A):c.6720C>G (p.Ala2240=) rs776767678 0.00004
NM_006015.6(ARID1A):c.376G>A (p.Gly126Ser) rs1400214289 0.00003
NM_006015.6(ARID1A):c.4530C>T (p.Asn1510=) rs200313047 0.00003
NM_006015.6(ARID1A):c.480C>T (p.Ala160=) rs775784171 0.00003
NM_006015.6(ARID1A):c.4947A>G (p.Thr1649=) rs201700725 0.00003
NM_006015.6(ARID1A):c.6331G>A (p.Val2111Ile) rs770028290 0.00003
NM_006015.6(ARID1A):c.1791C>T (p.Phe597=) rs375210036 0.00002
NM_006015.6(ARID1A):c.2328T>C (p.Pro776=) rs564495050 0.00002
NM_006015.6(ARID1A):c.36C>T (p.Ser12=) rs112262001 0.00002
NM_006015.6(ARID1A):c.6785C>T (p.Ser2262Leu) rs375849292 0.00002
NM_006015.6(ARID1A):c.239A>G (p.Asn80Ser) rs1553145891 0.00001
NM_006015.6(ARID1A):c.2668A>G (p.Met890Val) rs140664170 0.00001
NM_006015.6(ARID1A):c.6709G>A (p.Ala2237Thr) rs746165075 0.00001
NM_006015.6(ARID1A):c.114GGC[6] (p.Ala45dup) rs587779737
NM_006015.6(ARID1A):c.196C>T (p.Pro66Ser) rs962566886
NM_006015.6(ARID1A):c.249CGG[6] (p.Gly86_Gly87dup) rs1015322780
NM_006015.6(ARID1A):c.250_267del (p.Gly84_Gly89del) rs777773061
NM_006015.6(ARID1A):c.264C>T (p.Ala88=) rs765913797
NM_006015.6(ARID1A):c.3978GCA[9] (p.Gln1334dup) rs374564889
NM_006015.6(ARID1A):c.448T>C (p.Phe150Leu) rs2080267793
NM_006015.6(ARID1A):c.4768C>T (p.Pro1590Ser) rs370907880
NM_006015.6(ARID1A):c.483CGC[5] (p.Ala167dup) rs759913677
NM_006015.6(ARID1A):c.48GCC[4] (p.Pro21del) rs748085214
NM_006015.6(ARID1A):c.48GCC[7] (p.Pro20_Pro21dup) rs748085214
NM_006015.6(ARID1A):c.5287GAA[4] (p.Glu1767del) rs753766136
NM_006015.6(ARID1A):c.5438C>T (p.Pro1813Leu) rs1373371414
NM_006015.6(ARID1A):c.5717G>A (p.Arg1906Gln) rs41303631
NM_006015.6(ARID1A):c.581C>T (p.Pro194Leu) rs764060744
NM_006015.6(ARID1A):c.6612C>T (p.Ala2204=) rs752465350

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