ClinVar Miner

List of variants in gene ACTN2 reported as benign

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Gene type:
ClinVar version:
Total variants: 105
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HGVS dbSNP
NC_000001.11:g.236686164C>T rs75163151
NC_000001.11:g.236735384del rs143344656
NC_000001.11:g.236736600del rs11355106
NM_001103.2:c.378C>T
NM_001103.3(ACTN2):c.-22C>T rs138279482
NM_001103.3(ACTN2):c.-3G>T rs201920417
NM_001103.3(ACTN2):c.1107+123T>C rs7544174
NM_001103.3(ACTN2):c.1107+33A>C rs2288602
NM_001103.3(ACTN2):c.1108-5C>T rs369956166
NM_001103.3(ACTN2):c.1255+321G>A rs12737976
NM_001103.3(ACTN2):c.1256-79G>A rs3738543
NM_001103.3(ACTN2):c.126+14C>T rs373269478
NM_001103.3(ACTN2):c.126+157A>G rs12046163
NM_001103.3(ACTN2):c.126+331G>C rs644401
NM_001103.3(ACTN2):c.1296G>A (p.Ala432=) rs35956798
NM_001103.3(ACTN2):c.1298C>T (p.Ser433Leu) rs143749154
NM_001103.3(ACTN2):c.1332C>T (p.His444=) rs373709019
NM_001103.3(ACTN2):c.1341C>T (p.Phe447=) rs34785693
NM_001103.3(ACTN2):c.1371C>T (p.Arg457=) rs114008185
NM_001103.3(ACTN2):c.1383C>T (p.Ile461=) rs34827377
NM_001103.3(ACTN2):c.1406+8C>T rs397516567
NM_001103.3(ACTN2):c.1407-104T>C rs10802557
NM_001103.3(ACTN2):c.1407-128A>G rs75222641
NM_001103.3(ACTN2):c.1425C>T (p.Asp475=) rs148223734
NM_001103.3(ACTN2):c.1452G>A (p.Gln484=) rs200529923
NM_001103.3(ACTN2):c.1515+146G>T rs79149380
NM_001103.3(ACTN2):c.1515+15C>T rs368107695
NM_001103.3(ACTN2):c.1515+268C>T rs10802558
NM_001103.3(ACTN2):c.1515+47C>T rs79971593
NM_001103.3(ACTN2):c.1516-138G>A rs2297956
NM_001103.3(ACTN2):c.1516-205G>T rs3818884
NM_001103.3(ACTN2):c.1656+258C>T rs76505998
NM_001103.3(ACTN2):c.1656+275A>G rs4659712
NM_001103.3(ACTN2):c.1656+33A>G rs2297955
NM_001103.3(ACTN2):c.1656+92G>T rs3818883
NM_001103.3(ACTN2):c.1657-160G>C rs3738545
NM_001103.3(ACTN2):c.1657-16T>C rs148194175
NM_001103.3(ACTN2):c.1657-194C>T rs3738544
NM_001103.3(ACTN2):c.165C>T (p.Ala55=) rs193922634
NM_001103.3(ACTN2):c.1693C>T (p.Leu565=) rs546293678
NM_001103.3(ACTN2):c.1704G>A (p.Ala568=) rs369560444
NM_001103.3(ACTN2):c.1748A>G (p.Glu583Gly) rs200631005
NM_001103.3(ACTN2):c.1794G>A (p.Pro598=) rs137890030
NM_001103.3(ACTN2):c.1810A>G (p.Met604Val) rs35997569
NM_001103.3(ACTN2):c.1839+255G>A rs4659713
NM_001103.3(ACTN2):c.18C>A (p.Pro6=) rs368367224
NM_001103.3(ACTN2):c.18C>T (p.Pro6=) rs368367224
NM_001103.3(ACTN2):c.1932C>A (p.Ala644=) rs144680712
NM_001103.3(ACTN2):c.1974+10C>T rs368354944
NM_001103.3(ACTN2):c.1975-12C>T rs371352710
NM_001103.3(ACTN2):c.1975-314T>C rs2297861
NM_001103.3(ACTN2):c.1975-6C>G rs201255023
NM_001103.3(ACTN2):c.2147C>T (p.Thr716Met) rs193922635
NM_001103.3(ACTN2):c.2161C>A (p.Arg721Ser) rs149433837
NM_001103.3(ACTN2):c.2235A>G (p.Arg745=) rs141884271
NM_001103.3(ACTN2):c.2301+28A>G rs114906297
NM_001103.3(ACTN2):c.2367+108C>T rs12730862
NM_001103.3(ACTN2):c.2367+210A>G rs10925223
NM_001103.3(ACTN2):c.2367+301C>A rs4348712
NM_001103.3(ACTN2):c.2367+8A>G rs112714025
NM_001103.3(ACTN2):c.2368-17T>C rs78961574
NM_001103.3(ACTN2):c.241+131C>T rs2275399
NM_001103.3(ACTN2):c.241+135T>C rs10925203
NM_001103.3(ACTN2):c.241+302G>T rs34397827
NM_001103.3(ACTN2):c.242-84G>A rs1341865
NM_001103.3(ACTN2):c.2526+33A>G rs2282366
NM_001103.3(ACTN2):c.2526+8T>C rs760086675
NM_001103.3(ACTN2):c.2610G>A (p.Ser870=) rs12063382
NM_001103.3(ACTN2):c.2649G>A (p.Ala883=) rs146426213
NM_001103.3(ACTN2):c.351= (p.Ile117=) rs1341864
NM_001103.3(ACTN2):c.351C>T (p.Ile117=) rs1341864
NM_001103.3(ACTN2):c.361+96C>T rs41269355
NM_001103.3(ACTN2):c.362-165T>C rs1768053
NM_001103.3(ACTN2):c.362-244A>G rs1773444
NM_001103.3(ACTN2):c.378= (p.Asn126=) rs1341863
NM_001103.3(ACTN2):c.378T>C (p.Asn126=) rs1341863
NM_001103.3(ACTN2):c.441G>A (p.Ser147=) rs150182164
NM_001103.3(ACTN2):c.448+195G>T rs1341861
NM_001103.3(ACTN2):c.448+73G>A rs1341862
NM_001103.3(ACTN2):c.449-122G>C rs12081658
NM_001103.3(ACTN2):c.536+10C>T rs141219516
NM_001103.3(ACTN2):c.536+270G>A rs74146240
NM_001103.3(ACTN2):c.537-197A>G rs1768056
NM_001103.3(ACTN2):c.546T>C (p.Asp182=) rs34263845
NM_001103.3(ACTN2):c.615+15C>T rs369293885
NM_001103.3(ACTN2):c.697+33G>A rs819640
NM_001103.3(ACTN2):c.698-1068T>C rs16834301
NM_001103.3(ACTN2):c.698-1302A>G rs707203
NM_001103.3(ACTN2):c.698-1428C>T rs12569148
NM_001103.3(ACTN2):c.698-900T>C rs819643
NM_001103.3(ACTN2):c.783+22G>A rs2288600
NM_001103.3(ACTN2):c.784-404G>A rs7542508
NM_001103.3(ACTN2):c.877-238C>T rs4659711
NM_001103.3(ACTN2):c.877-42C>T rs7527525
NM_001103.3(ACTN2):c.877-6G>A rs397516585
NM_001103.3(ACTN2):c.877-8= rs2288601
NM_001103.3(ACTN2):c.877-8C>G rs2288601
NM_001103.3(ACTN2):c.877-99T>C rs11807254
NM_001103.3(ACTN2):c.918C>T (p.Asn306=) rs148646265
NM_001103.4(ACTN2):c.1423G>A (p.Asp475Asn) rs80257412
NM_001103.4(ACTN2):c.1426G>A (p.Ala476Thr) rs142943120
NM_001103.4(ACTN2):c.2076C>T (p.Ile692=) rs144122893
NM_001103.4(ACTN2):c.2139G>A (p.Thr713=) rs34975493
NM_001103.4(ACTN2):c.705G>C (p.Val235=) rs2288599
NM_001103.4(ACTN2):c.870G>A (p.Ala290=) rs116464082

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