ClinVar Miner

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

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Gene type:
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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_001101.5(ACTB):c.363+16C>T rs73332405 0.01128
NM_001101.5(ACTB):c.*280G>A rs11546905 0.01125
NM_001101.5(ACTB):c.*260G>A rs11546906 0.01124
NM_001101.5(ACTB):c.363+127C>A rs13447400 0.00828
NM_001101.5(ACTB):c.-6-309C>T rs13447393 0.00450
NM_001101.5(ACTB):c.426G>T (p.Leu142=) rs79074016 0.00353
NM_001101.5(ACTB):c.822C>A (p.Ile274=) rs377390140 0.00029
NM_001101.5(ACTB):c.364-44C>T rs13447403 0.00021
NM_001101.5(ACTB):c.1089C>T (p.Asp363=) rs370848417 0.00016
NM_001101.5(ACTB):c.453C>T (p.Ile151=) rs150837984 0.00012
NM_001101.5(ACTB):c.1011C>T (p.Tyr337=) rs748194756 0.00009
NM_001101.5(ACTB):c.280C>T (p.Leu94=) rs145281194 0.00009
NM_001101.5(ACTB):c.93C>T (p.Phe31=) rs748892906 0.00005
NM_001101.5(ACTB):c.-2C>G rs1406427507 0.00004
NM_001101.5(ACTB):c.36C>T (p.Asn12=) rs764325153 0.00004
NM_001101.5(ACTB):c.732C>T (p.Asp244=) rs552269338 0.00004
NM_001101.5(ACTB):c.-23T>C rs1057523391 0.00003
NM_001101.5(ACTB):c.198C>T (p.Thr66=) rs750565033 0.00003
NM_001101.5(ACTB):c.324C>T (p.Ala108=) rs746032511 0.00003
NM_001101.5(ACTB):c.363+15A>C rs772907450 0.00003
NM_001101.5(ACTB):c.720C>T (p.Tyr240=) rs145793213 0.00003
NM_001101.5(ACTB):c.858C>T (p.Asp286=) rs150105166 0.00003
NM_001101.5(ACTB):c.225C>T (p.Ile75=) rs759412044 0.00002
NM_001101.5(ACTB):c.657C>T (p.Val219=) rs143046775 0.00002
NM_001101.5(ACTB):c.-6-182G>A rs774049129 0.00001
NM_001101.5(ACTB):c.378C>T (p.Thr126=) rs1197579915 0.00001
NM_001101.5(ACTB):c.474G>A (p.Gly158=) rs141472083 0.00001
NM_001101.5(ACTB):c.526C>T (p.Leu176=) rs781543876 0.00001
NM_001101.5(ACTB):c.804C>T (p.Gly268=) rs770089307 0.00001
NM_001101.5(ACTB):c.*96dup rs372205322
NM_001101.5(ACTB):c.-50G>T rs1039646624
NM_001101.5(ACTB):c.-6-15C>G rs375195937
NM_001101.5(ACTB):c.-7+15C>G rs1057522749
NM_001101.5(ACTB):c.1116C>T (p.Arg372=)
NM_001101.5(ACTB):c.24C>A (p.Leu8=)
NM_001101.5(ACTB):c.306C>A (p.Pro102=) rs769021550
NM_001101.5(ACTB):c.364-4_364-3insAA rs751359436
NM_001101.5(ACTB):c.364-7C>T rs764266143
NM_001101.5(ACTB):c.424C>T (p.Leu142=)
NM_001101.5(ACTB):c.651C>T (p.Cys217=) rs1417923207
NM_001101.5(ACTB):c.783C>G (p.Leu261=) rs1057523531
NM_001101.5(ACTB):c.934A>C (p.Arg312=)

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