ClinVar Miner

List of variants in gene ARHGAP31 reported as benign by GeneDx

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_020754.4(ARHGAP31):c.1065= (p.Val355=) rs4688001 0.99997
NM_020754.4(ARHGAP31):c.2407G>A (p.Gly803Ser) rs3732413 0.83331
NM_020754.4(ARHGAP31):c.1927-149A>G rs4687855 0.80187
NM_020754.4(ARHGAP31):c.349-153A>G rs2318370 0.76002
NM_020754.4(ARHGAP31):c.1926+5A>G rs1463139 0.65282
NM_020754.4(ARHGAP31):c.1006+121A>G rs935616 0.59534
NM_020754.4(ARHGAP31):c.1926+11T>C rs1463138 0.48737
NM_020754.4(ARHGAP31):c.100+77A>T rs3732412 0.47316
NM_020754.4(ARHGAP31):c.101-330C>T rs6438524 0.41274
NM_020754.4(ARHGAP31):c.1926+89T>A rs12636976 0.38289
NM_020754.4(ARHGAP31):c.1070-92G>C rs10511390 0.30957
NM_020754.4(ARHGAP31):c.682+177G>A rs2077599 0.27289
NM_020754.4(ARHGAP31):c.1701G>A (p.Pro567=) rs2305249 0.15627
NM_020754.4(ARHGAP31):c.1926+87A>T rs74369586 0.14354
NM_020754.4(ARHGAP31):c.1070-287G>A rs75493824 0.14313
NM_020754.4(ARHGAP31):c.2778G>A (p.Ala926=) rs61740281 0.13385
NM_020754.4(ARHGAP31):c.3615C>T (p.Pro1205=) rs3732414 0.11361
NM_020754.4(ARHGAP31):c.203+66A>G rs17203055 0.09810
NM_020754.4(ARHGAP31):c.-38C>A rs72960626 0.08337
NM_020754.4(ARHGAP31):c.540-6C>T rs16829782 0.06792
NM_020754.4(ARHGAP31):c.432-100T>A rs73187863 0.06662
NM_020754.4(ARHGAP31):c.881+7G>A rs78837524 0.05675
NM_020754.4(ARHGAP31):c.349-113C>T rs79225620 0.04497
NM_020754.4(ARHGAP31):c.1007-112G>A rs78962354 0.04090
NM_020754.4(ARHGAP31):c.1926+163T>G rs72968486 0.02331
NM_020754.4(ARHGAP31):c.882-238C>G rs75191019 0.02316
NM_020754.4(ARHGAP31):c.*269A>G rs74767080 0.01996
NM_020754.4(ARHGAP31):c.1533A>G (p.Thr511=) rs77678258 0.01884
NM_020754.4(ARHGAP31):c.1700C>T (p.Pro567Leu) rs61744178 0.01870
NM_020754.4(ARHGAP31):c.432-237T>G rs115561893 0.01862
NM_020754.4(ARHGAP31):c.1491C>A (p.Arg497=) rs61747387 0.01861
NM_020754.4(ARHGAP31):c.101-37C>A rs113568026 0.01735
NM_020754.4(ARHGAP31):c.1614A>G (p.Glu538=) rs61744411 0.01720
NM_020754.4(ARHGAP31):c.101-294A>G rs143737497 0.01598
NM_020754.4(ARHGAP31):c.1007-210T>C rs76168470 0.01554
NM_020754.4(ARHGAP31):c.682+19A>C rs72966429 0.01526
NM_020754.4(ARHGAP31):c.101-49G>A rs116187120 0.01470
NM_020754.4(ARHGAP31):c.3256G>A (p.Ala1086Thr) rs61744168 0.00542
NM_020754.4(ARHGAP31):c.100+148del rs10707359
NM_020754.4(ARHGAP31):c.1926+97del rs149651758
NM_020754.4(ARHGAP31):c.432-284del rs10719267
NM_020754.4(ARHGAP31):c.432-287_432-284del rs10719267
NM_020754.4(ARHGAP31):c.540-44_540-43dup rs147532572
NM_020754.4(ARHGAP31):c.881+176C>T rs2241994

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