ClinVar Miner

List of variants in gene ACTN2 reported as benign for not provided

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Total variants: 56
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HGVS dbSNP
NC_000001.11:g.236686164C>T
NC_000001.11:g.236735384del
NC_000001.11:g.236736600del
NM_001103.3(ACTN2):c.1107+123T>C
NM_001103.3(ACTN2):c.1107+33A>C
NM_001103.3(ACTN2):c.1255+321G>A
NM_001103.3(ACTN2):c.1256-79G>A
NM_001103.3(ACTN2):c.126+157A>G
NM_001103.3(ACTN2):c.126+331G>C
NM_001103.3(ACTN2):c.1371C>T (p.Arg457=) rs114008185
NM_001103.3(ACTN2):c.1407-104T>C
NM_001103.3(ACTN2):c.1407-128A>G
NM_001103.3(ACTN2):c.1423G>A (p.Asp475Asn) rs80257412
NM_001103.3(ACTN2):c.1515+146G>T
NM_001103.3(ACTN2):c.1515+268C>T
NM_001103.3(ACTN2):c.1515+47C>T
NM_001103.3(ACTN2):c.1516-138G>A
NM_001103.3(ACTN2):c.1516-205G>T
NM_001103.3(ACTN2):c.1656+258C>T
NM_001103.3(ACTN2):c.1656+275A>G
NM_001103.3(ACTN2):c.1656+33A>G
NM_001103.3(ACTN2):c.1656+92G>T
NM_001103.3(ACTN2):c.1657-160G>C
NM_001103.3(ACTN2):c.1657-194C>T
NM_001103.3(ACTN2):c.1810A>G (p.Met604Val) rs35997569
NM_001103.3(ACTN2):c.1839+255G>A
NM_001103.3(ACTN2):c.1975-314T>C
NM_001103.3(ACTN2):c.2301+28A>G
NM_001103.3(ACTN2):c.2367+108C>T
NM_001103.3(ACTN2):c.2367+210A>G
NM_001103.3(ACTN2):c.2367+301C>A
NM_001103.3(ACTN2):c.241+131C>T
NM_001103.3(ACTN2):c.241+135T>C
NM_001103.3(ACTN2):c.241+302G>T
NM_001103.3(ACTN2):c.242-84G>A
NM_001103.3(ACTN2):c.2526+33A>G
NM_001103.3(ACTN2):c.361+96C>T
NM_001103.3(ACTN2):c.362-165T>C
NM_001103.3(ACTN2):c.362-244A>G
NM_001103.3(ACTN2):c.441G>A (p.Ser147=) rs150182164
NM_001103.3(ACTN2):c.448+195G>T
NM_001103.3(ACTN2):c.448+73G>A
NM_001103.3(ACTN2):c.449-122G>C
NM_001103.3(ACTN2):c.536+270G>A
NM_001103.3(ACTN2):c.537-197A>G
NM_001103.3(ACTN2):c.697+33G>A
NM_001103.3(ACTN2):c.698-1068T>C
NM_001103.3(ACTN2):c.698-1302A>G
NM_001103.3(ACTN2):c.698-1428C>T
NM_001103.3(ACTN2):c.698-900T>C
NM_001103.3(ACTN2):c.705G>C (p.Val235=) rs2288599
NM_001103.3(ACTN2):c.783+22G>A rs2288600
NM_001103.3(ACTN2):c.784-404G>A
NM_001103.3(ACTN2):c.877-238C>T
NM_001103.3(ACTN2):c.877-42C>T
NM_001103.3(ACTN2):c.877-99T>C

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