ClinVar Miner

List of variants in gene ACTG1 reported as likely benign for not provided

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Gene type:
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Total variants: 101
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HGVS dbSNP gnomAD frequency
NM_001614.5(ACTG1):c.1026T>C (p.Gly342=) rs1139406 0.04214
NM_001614.5(ACTG1):c.1014G>A (p.Ser338=) rs1139807 0.04188
NM_001614.5(ACTG1):c.363+123C>A rs117809695 0.01608
NM_001614.5(ACTG1):c.399C>T (p.Tyr133=) rs2230158 0.01567
NM_001614.5(ACTG1):c.729C>T (p.Pro243=) rs2230159 0.01563
NM_001614.5(ACTG1):c.*134C>T rs28478053 0.01352
NM_001614.5(ACTG1):c.177G>A (p.Gln59=) rs11549220 0.01161
NC_000017.11:g.81512884C>A rs555771133 0.00997
NM_001614.5(ACTG1):c.-6-3C>T rs140724578 0.00374
NM_001614.5(ACTG1):c.363+127C>T rs143384856 0.00303
NM_001614.5(ACTG1):c.714G>A (p.Lys238=) rs11549173 0.00287
NM_001614.5(ACTG1):c.780G>A (p.Ala260=) rs140846345 0.00287
NM_001614.5(ACTG1):c.471C>T (p.Asp157=) rs11549222 0.00264
NM_001614.5(ACTG1):c.684C>T (p.Ala228=) rs143125497 0.00195
NM_001614.5(ACTG1):c.*227C>T rs184661152 0.00137
NM_001614.5(ACTG1):c.18C>T (p.Ala6=) rs145211830 0.00128
NM_001614.5(ACTG1):c.-42G>A rs782068009 0.00106
NM_001614.5(ACTG1):c.1029C>T (p.Gly343=) rs143659814 0.00106
NM_001614.5(ACTG1):c.531T>C (p.Arg177=) rs143851458 0.00106
NM_001614.5(ACTG1):c.-27C>T rs552393684 0.00060
NM_001614.5(ACTG1):c.774G>A (p.Pro258=) rs61997068 0.00053
NM_001614.5(ACTG1):c.-26G>A rs527479909 0.00047
NM_001614.5(ACTG1):c.-6-16A>G rs373198187 0.00041
NM_001614.5(ACTG1):c.*259C>T rs540974291 0.00040
NM_001614.5(ACTG1):c.1107C>T (p.Ile369=) rs372665803 0.00035
NM_001614.5(ACTG1):c.-43T>A rs1057522087 0.00031
NM_001614.5(ACTG1):c.180C>T (p.Ser60=) rs144338558 0.00031
NM_001614.5(ACTG1):c.364-8C>T rs201748657 0.00031
NM_001614.5(ACTG1):c.126C>T (p.Gly42=) rs11549197 0.00029
NM_001614.5(ACTG1):c.654C>T (p.Tyr218=) rs182162229 0.00024
NM_001614.5(ACTG1):c.546C>T (p.Gly182=) rs61997063 0.00023
NM_001614.5(ACTG1):c.210C>T (p.Pro70=) rs201275526 0.00021
NM_001614.5(ACTG1):c.364-116C>G rs782603481 0.00021
NM_001614.5(ACTG1):c.-28C>T rs782317187 0.00020
NM_001614.5(ACTG1):c.*112C>T rs368494254 0.00019
NM_001614.5(ACTG1):c.803-3T>C rs369438865 0.00019
NM_001614.5(ACTG1):c.803-29C>T rs189965694 0.00016
NM_001614.5(ACTG1):c.984+7C>T rs369691985 0.00011
NM_001614.5(ACTG1):c.564C>T (p.Tyr188=) rs141964376 0.00009
NM_001614.5(ACTG1):c.858C>T (p.Asp286=) rs201277295 0.00009
NM_001614.5(ACTG1):c.364-20C>T rs138210010 0.00008
NM_001614.5(ACTG1):c.486G>A (p.Thr162=) rs782442814 0.00008
NM_001614.5(ACTG1):c.669C>T (p.Phe223=) rs373099591 0.00008
NM_001614.5(ACTG1):c.816C>T (p.Cys272=) rs376841359 0.00008
NM_001614.5(ACTG1):c.168C>T (p.Asp56=) rs368299537 0.00007
NM_001614.5(ACTG1):c.124-9C>T rs376850595 0.00006
NM_001614.5(ACTG1):c.267C>T (p.Thr89=) rs140398667 0.00006
NM_001614.5(ACTG1):c.351G>A (p.Glu117=) rs200772616 0.00006
NM_001614.5(ACTG1):c.363+7C>G rs782205549 0.00006
NM_001614.5(ACTG1):c.609G>A (p.Thr203=) rs148528303 0.00006
NM_001614.5(ACTG1):c.624C>T (p.Ile208=) rs370369574 0.00006
NM_001614.5(ACTG1):c.690C>T (p.Ala230=) rs11549213 0.00006
NM_001614.5(ACTG1):c.924C>T (p.Gly308=) rs371738013 0.00005
NM_001614.5(ACTG1):c.627G>A (p.Val209=) rs1381583619 0.00004
NM_001614.5(ACTG1):c.666C>T (p.Asp222=) rs376839455 0.00004
NM_001614.5(ACTG1):c.1053C>T (p.Thr351=) rs148267855 0.00003
NM_001614.5(ACTG1):c.498C>T (p.Tyr166=) rs373572370 0.00003
NM_001614.5(ACTG1):c.534G>A (p.Leu178=) rs140035543 0.00003
NM_001614.5(ACTG1):c.696C>T (p.Ser232=) rs202155328 0.00003
NM_001614.5(ACTG1):c.720C>T (p.Tyr240=) rs376038784 0.00003
NM_001614.5(ACTG1):c.802+20G>A rs782239781 0.00003
NM_001614.5(ACTG1):c.1023C>T (p.Ile341=) rs140865670 0.00002
NM_001614.5(ACTG1):c.429C>T (p.Tyr143=) rs782719226 0.00002
NM_001614.5(ACTG1):c.945G>A (p.Lys315=) rs727502881 0.00002
NM_001614.5(ACTG1):c.*6C>G rs782239083 0.00001
NM_001614.5(ACTG1):c.1104C>T (p.Ser368=) rs1433816139 0.00001
NM_001614.5(ACTG1):c.138C>T (p.Gly46=) rs374907377 0.00001
NM_001614.5(ACTG1):c.310C>T (p.Leu104=) rs782549602 0.00001
NM_001614.5(ACTG1):c.378C>T (p.Thr126=) rs11549201 0.00001
NM_001614.5(ACTG1):c.390G>A (p.Pro130=) rs561518636 0.00001
NM_001614.5(ACTG1):c.888C>T (p.Asn296=) rs782140372 0.00001
NM_001614.5(ACTG1):c.936G>A (p.Arg312=) rs1555666472 0.00001
NC_000017.11:g.81512817C>G rs542961891
NM_001614.5(ACTG1):c.*130G>A rs782530017
NM_001614.5(ACTG1):c.*194A>C rs537839620
NM_001614.5(ACTG1):c.-48C>A rs567737230
NM_001614.5(ACTG1):c.-5T>C rs782246678
NM_001614.5(ACTG1):c.-6-13C>T rs200070347
NM_001614.5(ACTG1):c.-6-7C>T rs199699427
NM_001614.5(ACTG1):c.1089C>T (p.Asp363=)
NM_001614.5(ACTG1):c.123G>A (p.Gln41=)
NM_001614.5(ACTG1):c.124-4G>C rs782481421
NM_001614.5(ACTG1):c.165C>A (p.Gly55=) rs146402466
NM_001614.5(ACTG1):c.165C>G (p.Gly55=) rs146402466
NM_001614.5(ACTG1):c.174C>G (p.Ala58=) rs782205858
NM_001614.5(ACTG1):c.234C>T (p.Asn78=)
NM_001614.5(ACTG1):c.318C>G (p.Thr106=) rs372370199
NM_001614.5(ACTG1):c.324C>T (p.Ala108=) rs550936698
NM_001614.5(ACTG1):c.363+111C>T rs780514084
NM_001614.5(ACTG1):c.363+72C>T rs782504453
NM_001614.5(ACTG1):c.414C>T (p.Ala138=) rs143978597
NM_001614.5(ACTG1):c.492C>T (p.Pro164=) rs1207365676
NM_001614.5(ACTG1):c.526C>G (p.Leu176Val) rs782088589
NM_001614.5(ACTG1):c.576C>T (p.Ile192=) rs186443800
NM_001614.5(ACTG1):c.648G>A (p.Leu216=)
NM_001614.5(ACTG1):c.702T>C (p.Ser234=)
NM_001614.5(ACTG1):c.766C>A (p.Arg256=) rs281875329
NM_001614.5(ACTG1):c.981C>T (p.Ile327=) rs782329552
NM_001614.5(ACTG1):c.984+13dup rs1555666452
NM_001614.5(ACTG1):c.985-5dup rs782289893
NM_001614.5(ACTG1):c.996C>A (p.Pro332=) rs200089021

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