ClinVar Miner

List of variants in gene ARID1A reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006015.6(ARID1A):c.4004+35C>T rs35428899 0.02027
NM_006015.6(ARID1A):c.3199-216dup rs552879011 0.00898
NM_006015.6(ARID1A):c.3199-74G>C rs114921256 0.00600
NM_006015.6(ARID1A):c.2419+298del rs150956702 0.00591
NM_006015.6(ARID1A):c.6586C>T (p.Leu2196=) rs149633292 0.00468
NC_000001.11:g.26695829G>A rs573303670 0.00395
NC_000001.11:g.26695894T>C rs565325921 0.00374
NM_006015.6(ARID1A):c.2733-290A>G rs144090778 0.00361
NM_006015.6(ARID1A):c.1350+25G>C rs117342430 0.00146
NM_006015.6(ARID1A):c.2615T>C (p.Met872Thr) rs140568310 0.00040
NM_006015.6(ARID1A):c.3199-25C>T rs375583580 0.00037
NM_006015.6(ARID1A):c.5491C>G (p.Leu1831Val) rs150534917 0.00020
NM_006015.6(ARID1A):c.2698G>A (p.Ala900Thr) rs138418893 0.00019
NM_006015.6(ARID1A):c.6582C>T (p.Asn2194=) rs138280531 0.00019
NM_006015.6(ARID1A):c.5449G>A (p.Val1817Ile) rs375250508 0.00016
NM_006015.6(ARID1A):c.*10G>T rs372029026 0.00015
NM_006015.6(ARID1A):c.6027C>T (p.Leu2009=) rs771725023 0.00015
NM_006015.6(ARID1A):c.375T>C (p.Gly125=) rs1285709722 0.00013
NM_006015.6(ARID1A):c.405T>G (p.Pro135=) rs922780561 0.00013
NM_006015.6(ARID1A):c.1175C>A (p.Pro392His) rs199906671 0.00011
NM_006015.6(ARID1A):c.456A>G (p.Gln152=) rs1043397333 0.00010
NM_006015.6(ARID1A):c.*5C>T rs201289176 0.00009
NM_006015.6(ARID1A):c.3978G>A (p.Pro1326=) rs370696498 0.00008
NM_006015.6(ARID1A):c.4773G>T (p.Leu1591=) rs779619447 0.00008
NM_006015.6(ARID1A):c.372C>T (p.Gly124=) rs1005812119 0.00006
NM_006015.6(ARID1A):c.3967C>T (p.Arg1323Cys) rs587778051 0.00005
NM_006015.6(ARID1A):c.4576G>A (p.Val1526Met) rs773815689 0.00005
NM_006015.6(ARID1A):c.6708C>T (p.Arg2236=) rs757672227 0.00005
NM_006015.6(ARID1A):c.111C>T (p.Gly37=) rs1057522894 0.00004
NM_006015.6(ARID1A):c.5647A>T (p.Thr1883Ser) rs150076443 0.00004
NM_006015.6(ARID1A):c.6730G>T (p.Val2244Leu) rs372878743 0.00004
NM_006015.6(ARID1A):c.6807A>G (p.Ser2269=) rs141124050 0.00004
NM_006015.6(ARID1A):c.1292C>T (p.Pro431Leu) rs572680423 0.00003
NM_006015.6(ARID1A):c.2091G>A (p.Pro697=) rs990716737 0.00003
NM_006015.6(ARID1A):c.376G>A (p.Gly126Ser) rs1400214289 0.00003
NM_006015.6(ARID1A):c.4564G>A (p.Ala1522Thr) rs199776442 0.00003
NM_006015.6(ARID1A):c.482T>C (p.Val161Ala) rs1427038078 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.2881A>C (p.Met961Leu) rs201899604 0.00002
NM_006015.6(ARID1A):c.5497C>T (p.Arg1833Cys) rs372213935 0.00002
NM_006015.6(ARID1A):c.6613G>A (p.Ala2205Thr) rs141992367 0.00002
NM_006015.6(ARID1A):c.1380C>T (p.Ser460=) rs752841889 0.00001
NM_006015.6(ARID1A):c.2229A>G (p.Gln743=) rs746513616 0.00001
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.299T>C (p.Leu100Pro) rs1570538685 0.00001
NM_006015.6(ARID1A):c.437C>T (p.Pro146Leu) rs781072025 0.00001
NM_006015.6(ARID1A):c.5124+123C>G rs745869437 0.00001
NM_006015.6(ARID1A):c.6070C>T (p.Arg2024Trp) rs2081175768 0.00001
NM_006015.6(ARID1A):c.6709G>A (p.Ala2237Thr) rs746165075 0.00001
NM_006015.6(ARID1A):c.*37C>G rs375168652
NM_006015.6(ARID1A):c.*3_*13del (p.Ter2286=) rs1027841569
NM_006015.6(ARID1A):c.114GGC[6] (p.Ala45dup) rs587779737
NM_006015.6(ARID1A):c.1803+274TTTTA[6] rs536029374
NM_006015.6(ARID1A):c.2109C>T (p.Pro703=) rs200927747
NM_006015.6(ARID1A):c.250_267del (p.Gly84_Gly89del) rs777773061
NM_006015.6(ARID1A):c.261_278del (p.Ala88_Gly93del) rs749452696
NM_006015.6(ARID1A):c.263_277del (p.Ala88_Gly92del) rs1191458952
NM_006015.6(ARID1A):c.2732+160G>A rs140476492
NM_006015.6(ARID1A):c.3198+10C>T rs376389652
NM_006015.6(ARID1A):c.3975C>G (p.Pro1325=) rs148038965
NM_006015.6(ARID1A):c.439G>C (p.Ala147Pro) rs2080267597
NM_006015.6(ARID1A):c.48GCC[3] (p.Pro20_Pro21del) rs748085214
NM_006015.6(ARID1A):c.48GCC[4] (p.Pro21del) rs748085214
NM_006015.6(ARID1A):c.48GCC[6] (p.Pro21dup) rs748085214
NM_006015.6(ARID1A):c.48GCC[7] (p.Pro20_Pro21dup) rs748085214
NM_006015.6(ARID1A):c.4993+22G>C rs371056521
NM_006015.6(ARID1A):c.5344G>C (p.Val1782Leu) rs775923229
NM_006015.6(ARID1A):c.5542G>T (p.Gly1848Trp) rs140055856
NM_006015.6(ARID1A):c.5717G>A (p.Arg1906Gln) rs41303631
NM_006015.6(ARID1A):c.5719A>T (p.Ile1907Phe) rs139230162
NM_006015.6(ARID1A):c.581C>T (p.Pro194Leu) rs764060744
NM_006015.6(ARID1A):c.591G>T (p.Gly197=) rs752595380
NM_006015.6(ARID1A):c.66G>C (p.Ser22=) rs2124740000

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.