ClinVar Miner

List of variants in gene ARID2 reported as likely benign for not provided

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Gene type:
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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_152641.4(ARID2):c.1718C>T (p.Thr573Met) rs76994389 0.00270
NM_152641.4(ARID2):c.4146C>T (p.Ser1382=) rs143660736 0.00128
NM_152641.4(ARID2):c.4705G>A (p.Ala1569Thr) rs78712333 0.00128
NM_152641.4(ARID2):c.4510C>T (p.Arg1504Trp) rs140500006 0.00112
NM_152641.4(ARID2):c.1808C>T (p.Ala603Val) rs144928351 0.00100
NM_152641.4(ARID2):c.1518G>A (p.Ala506=) rs148462633 0.00096
NM_152641.4(ARID2):c.1472C>G (p.Thr491Ser) rs149755754 0.00071
NM_152641.4(ARID2):c.4227T>C (p.Gly1409=) rs61745993 0.00043
NM_152641.4(ARID2):c.4945G>C (p.Val1649Leu) rs201268655 0.00036
NM_152641.4(ARID2):c.2466C>T (p.Ile822=) rs141401951 0.00034
NM_152641.4(ARID2):c.4311G>A (p.Ala1437=) rs138606745 0.00025
NM_152641.4(ARID2):c.2970G>A (p.Ser990=) rs78234941 0.00022
NM_152641.4(ARID2):c.4995G>C (p.Gly1665=) rs141708323 0.00021
NM_152641.4(ARID2):c.4853C>A (p.Ser1618Tyr) rs144553917 0.00013
NM_152641.4(ARID2):c.4911G>A (p.Gln1637=) rs774549564 0.00011
NM_152641.4(ARID2):c.28C>A (p.Pro10Thr) rs560068535 0.00007
NM_152641.4(ARID2):c.1359T>C (p.Asp453=) rs138343177 0.00006
NM_152641.4(ARID2):c.3068C>T (p.Pro1023Leu) rs577713771 0.00004
NM_152641.4(ARID2):c.1374C>T (p.Gly458=) rs201532081 0.00002
NM_152641.4(ARID2):c.1913-8A>G rs1022277868 0.00001
NM_152641.4(ARID2):c.2097A>G (p.Pro699=) rs751006445 0.00001
NM_152641.4(ARID2):c.2112A>G (p.Gln704=) rs373556686 0.00001
NM_152641.4(ARID2):c.2853A>G (p.Pro951=) rs962804031 0.00001
NM_152641.4(ARID2):c.3183A>G (p.Lys1061=) rs750172435 0.00001
NM_152641.4(ARID2):c.4257T>A (p.Pro1419=) rs754474375 0.00001
NM_152641.4(ARID2):c.4512G>A (p.Arg1504=) rs746999369 0.00001
NM_152641.4(ARID2):c.4774-6T>C rs942806319 0.00001
NM_152641.4(ARID2):c.1236G>A (p.Val412=) rs746373817
NM_152641.4(ARID2):c.1499C>G (p.Ala500Gly)
NM_152641.4(ARID2):c.1692A>C (p.Ser564=) rs776411576
NM_152641.4(ARID2):c.1952A>C (p.Gln651Pro)
NM_152641.4(ARID2):c.2067A>G (p.Ser689=) rs1592118877
NM_152641.4(ARID2):c.2219A>G (p.Gln740Arg)
NM_152641.4(ARID2):c.2647G>A (p.Val883Ile) rs1332955123
NM_152641.4(ARID2):c.2664C>G (p.Ala888=)
NM_152641.4(ARID2):c.2727A>G (p.Thr909=)
NM_152641.4(ARID2):c.2797G>A (p.Ala933Thr)
NM_152641.4(ARID2):c.3342A>G (p.Gln1114=)
NM_152641.4(ARID2):c.3354G>A (p.Gln1118=) rs1415583899
NM_152641.4(ARID2):c.3429G>T (p.Val1143=) rs1592120553
NM_152641.4(ARID2):c.3438G>A (p.Ser1146=)
NM_152641.4(ARID2):c.3617C>T (p.Thr1206Met)
NM_152641.4(ARID2):c.3647C>T (p.Thr1216Met)
NM_152641.4(ARID2):c.3687A>G (p.Ser1229=)
NM_152641.4(ARID2):c.3689G>A (p.Cys1230Tyr)
NM_152641.4(ARID2):c.3981A>G (p.Ser1327=) rs776048474
NM_152641.4(ARID2):c.3981A>T (p.Ser1327=) rs776048474
NM_152641.4(ARID2):c.4029A>G (p.Gln1343=) rs1239037267
NM_152641.4(ARID2):c.4061G>A (p.Arg1354Lys) rs1376454522
NM_152641.4(ARID2):c.4094A>G (p.Asp1365Gly)
NM_152641.4(ARID2):c.419-5G>A
NM_152641.4(ARID2):c.4511G>A (p.Arg1504Gln)
NM_152641.4(ARID2):c.4581C>G (p.Val1527=)
NM_152641.4(ARID2):c.4581C>T (p.Val1527=) rs373420723
NM_152641.4(ARID2):c.4692T>C (p.Thr1564=) rs1042420209
NM_152641.4(ARID2):c.4777A>G (p.Thr1593Ala) rs771509959
NM_152641.4(ARID2):c.4789C>T (p.Pro1597Ser)
NM_152641.4(ARID2):c.4824C>T (p.Asn1608=) rs1592127267
NM_152641.4(ARID2):c.5244A>G (p.Ser1748=)

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