ClinVar Miner

List of variants in gene ARID1A reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 39
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HGVS dbSNP gnomAD frequency
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.5336A>G (p.Glu1779Gly) rs140946580 0.00112
NM_006015.6(ARID1A):c.472C>T (p.Pro158Ser) rs567246585 0.00088
NM_006015.6(ARID1A):c.3792C>T (p.Ala1264=) rs142429183 0.00061
NM_006015.6(ARID1A):c.3762C>T (p.Gly1254=) rs138814830 0.00060
NM_006015.6(ARID1A):c.4563C>T (p.Pro1521=) rs149095176 0.00058
NM_006015.6(ARID1A):c.4053C>T (p.Gly1351=) rs200122106 0.00031
NM_006015.6(ARID1A):c.6582C>T (p.Asn2194=) rs138280531 0.00020
NM_006015.6(ARID1A):c.2718C>G (p.Asn906Lys) rs201864573 0.00016
NM_006015.6(ARID1A):c.405T>G (p.Pro135=) rs922780561 0.00013
NM_006015.6(ARID1A):c.2204G>A (p.Ser735Asn) rs142353005 0.00011
NM_006015.6(ARID1A):c.6708C>T (p.Arg2236=) rs757672227 0.00005
NM_006015.6(ARID1A):c.4081A>G (p.Met1361Val) rs770710220 0.00004
NM_006015.6(ARID1A):c.6331G>A (p.Val2111Ile) rs770028290 0.00004
NM_006015.6(ARID1A):c.480C>T (p.Ala160=) rs775784171 0.00003
NM_006015.6(ARID1A):c.5299G>C (p.Glu1767Gln) rs1408637499 0.00002
NM_006015.6(ARID1A):c.357G>A (p.Glu119=) rs757540852 0.00001
NM_006015.6(ARID1A):c.1224G>A (p.Pro408=)
NM_006015.6(ARID1A):c.1362T>C (p.Tyr454=)
NM_006015.6(ARID1A):c.1469C>T (p.Pro490Leu)
NM_006015.6(ARID1A):c.1473C>T (p.Ser491=)
NM_006015.6(ARID1A):c.1616C>T (p.Ser539Leu)
NM_006015.6(ARID1A):c.1764G>A (p.Gln588=)
NM_006015.6(ARID1A):c.2388T>C (p.Tyr796=)
NM_006015.6(ARID1A):c.2449G>C (p.Ala817Pro) rs1553152137
NM_006015.6(ARID1A):c.2550T>C (p.Tyr850=)
NM_006015.6(ARID1A):c.369C>T (p.Gly123=)
NM_006015.6(ARID1A):c.448T>C (p.Phe150Leu) rs2080267793
NM_006015.6(ARID1A):c.4530C>T (p.Asn1510=)
NM_006015.6(ARID1A):c.5028C>T (p.Leu1676=)
NM_006015.6(ARID1A):c.5300A>T (p.Glu1767Val)
NM_006015.6(ARID1A):c.5301A>T (p.Glu1767Asp)
NM_006015.6(ARID1A):c.5398A>C (p.Asn1800His)
NM_006015.6(ARID1A):c.5719A>T (p.Ile1907Phe) rs139230162
NM_006015.6(ARID1A):c.6231C>T (p.Pro2077=)
NM_006015.6(ARID1A):c.624C>A (p.Pro208=) rs770301214
NM_006015.6(ARID1A):c.6720C>G (p.Ala2240=)
NM_006015.6(ARID1A):c.6735C>T (p.Asp2245=)

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