ClinVar Miner

List of variants in gene ANO3 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_031418.4(ANO3):c.2764-308G>A rs72883212 0.02335
NM_031418.4(ANO3):c.2657+44A>T rs72881793 0.02323
NM_031418.4(ANO3):c.591+243G>A rs117806277 0.02271
NM_031418.4(ANO3):c.591+270A>G rs117975000 0.02268
NM_031418.4(ANO3):c.1290-6C>T rs770584529 0.02039
NM_031418.4(ANO3):c.2043+279A>T rs367984233 0.01830
NM_031418.4(ANO3):c.*192C>T rs116932997 0.01628
NM_031418.4(ANO3):c.1874-239C>A rs77132774 0.01562
NM_031418.4(ANO3):c.1873+135G>A rs76835196 0.01448
NM_031418.4(ANO3):c.1672-199A>G rs185108103 0.01414
NM_031418.4(ANO3):c.1836+19A>G rs78440820 0.01320
NM_031418.4(ANO3):c.1837-180A>C rs143194925 0.01275
NM_031418.4(ANO3):c.2141+258G>C rs114828690 0.01275
NM_031418.4(ANO3):c.2577-240A>G rs116010135 0.01263
NM_031418.4(ANO3):c.869+226C>T rs118009539 0.01135
NM_031418.4(ANO3):c.1448-206A>T rs74567353 0.00895
NM_031418.4(ANO3):c.2429-308C>T rs146935618 0.00877
NM_031418.4(ANO3):c.432+165A>G rs113967511 0.00857
NM_031418.4(ANO3):c.693-113A>G rs114500569 0.00801
NM_031418.4(ANO3):c.-54C>T rs149195780 0.00772
NM_031418.4(ANO3):c.2811C>T (p.Asp937=) rs117748217 0.00742
NM_031418.4(ANO3):c.1968C>T (p.Ile656=) rs149050831 0.00597
NM_031418.4(ANO3):c.2576+80T>C rs113220557 0.00538
NM_031418.4(ANO3):c.1290-44T>C rs150168906 0.00507
NM_031418.4(ANO3):c.1985+28C>T rs149131975 0.00479
NM_031418.4(ANO3):c.164C>T (p.Ser55Phe) rs61746297 0.00470
NM_031418.4(ANO3):c.433-126C>T rs187779325 0.00425
NM_031418.4(ANO3):c.692+148T>C rs527286850 0.00321
NM_031418.4(ANO3):c.714C>T (p.Asp238=) rs146532706 0.00288
NM_031418.4(ANO3):c.1032+15C>T rs187545947 0.00223
NM_031418.4(ANO3):c.2817A>G (p.Pro939=) rs150506041 0.00137
NM_031418.4(ANO3):c.693-154C>T rs548723055 0.00095
NM_031418.4(ANO3):c.1915C>T (p.Leu639=) rs149866447 0.00043
NM_031418.4(ANO3):c.1290-13G>A rs56325113 0.00030
NM_031418.4(ANO3):c.407C>A (p.Ser136Tyr) rs199574429 0.00021
NM_031418.4(ANO3):c.295C>A (p.Leu99Ile) rs370404701 0.00020
NM_031418.4(ANO3):c.2373A>T (p.Ala791=) rs141587028 0.00019
NM_031418.4(ANO3):c.704A>G (p.Tyr235Cys) rs144792604 0.00014
NM_031418.4(ANO3):c.2906G>A (p.Arg969Gln) rs777387236 0.00004
NM_031418.4(ANO3):c.1033-4G>T rs749899725 0.00002
NM_031418.4(ANO3):c.1112G>A (p.Arg371His) rs187173978 0.00002
NM_031418.4(ANO3):c.2412C>G (p.Ala804=) rs775827602 0.00002
NM_031418.4(ANO3):c.2328T>C (p.Pro776=) rs754631898 0.00001
NM_031418.4(ANO3):c.-143G>A rs114059269
NM_031418.4(ANO3):c.1290-14del rs376265231
NM_031418.4(ANO3):c.1290-20dup rs367822925
NM_031418.4(ANO3):c.1290-26_1290-25insTTTTT rs201093158
NM_031418.4(ANO3):c.1290-27_1290-26dup rs201093158
NM_031418.4(ANO3):c.1290-5_1290-4del rs202169392
NM_031418.4(ANO3):c.1290-7del rs1006647820
NM_031418.4(ANO3):c.1494C>A (p.Thr498=) rs148526395
NM_031418.4(ANO3):c.2027G>A (p.Arg676Gln)
NM_031418.4(ANO3):c.2275+313_2275+322del rs1231554094
NM_031418.4(ANO3):c.2566C>T (p.Pro856Ser)
NM_031418.4(ANO3):c.313+88dup rs980416807
NM_031418.4(ANO3):c.314-276G>A rs17309048
NM_031418.4(ANO3):c.46+137_46+139dup rs56225203
NM_031418.4(ANO3):c.46+138_46+139dup rs56225203
NM_031418.4(ANO3):c.737+119G>T rs111594806

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