ClinVar Miner

List of variants in gene ACTG1 reported as benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_001614.5(ACTG1):c.1014G>A (p.Ser338=) rs1139807
NM_001614.5(ACTG1):c.1026T>C (p.Gly342=) rs1139406
NM_001614.5(ACTG1):c.1029C>T (p.Gly343=) rs143659814
NM_001614.5(ACTG1):c.1113C>T (p.His371=) rs117765323
NM_001614.5(ACTG1):c.1128A>G (p.Ter376=) rs11549223
NM_001614.5(ACTG1):c.165C>T (p.Gly55=) rs146402466
NM_001614.5(ACTG1):c.177G>A (p.Gln59=) rs11549220
NM_001614.5(ACTG1):c.18C>T (p.Ala6=) rs145211830
NM_001614.5(ACTG1):c.228C>T (p.Val76=) rs143028649
NM_001614.5(ACTG1):c.345C>T (p.Asn115=) rs149057480
NM_001614.5(ACTG1):c.363+7C>G rs782205549
NM_001614.5(ACTG1):c.399C>T (p.Tyr133=) rs2230158
NM_001614.5(ACTG1):c.39C>T (p.Gly13=) rs146865914
NM_001614.5(ACTG1):c.414C>T (p.Ala138=) rs143978597
NM_001614.5(ACTG1):c.471C>T (p.Asp157=) rs11549222
NM_001614.5(ACTG1):c.531T>C (p.Arg177=) rs143851458
NM_001614.5(ACTG1):c.546C>T (p.Gly182=) rs61997063
NM_001614.5(ACTG1):c.558C>T (p.Thr186=) rs142893042
NM_001614.5(ACTG1):c.684C>T (p.Ala228=) rs143125497
NM_001614.5(ACTG1):c.714G>A (p.Lys238=) rs11549173
NM_001614.5(ACTG1):c.729C>T (p.Pro243=) rs2230159
NM_001614.5(ACTG1):c.72C>T (p.Asp24=) rs139517777
NM_001614.5(ACTG1):c.735C>T (p.Gly245=) rs186289501
NM_001614.5(ACTG1):c.774G>A (p.Pro258=) rs61997068
NM_001614.5(ACTG1):c.780G>A (p.Ala260=) rs140846345
NM_001614.5(ACTG1):c.803-6C>T rs199600452
NM_001614.5(ACTG1):c.877C>T (p.Leu293=) rs143205514
NM_001614.5(ACTG1):c.909C>T (p.Thr303=) rs187127467
NM_001614.5(ACTG1):c.918C>T (p.Tyr306=) rs1139405
NM_001614.5(ACTG1):c.930C>T (p.Ala310=) rs1135989
NM_001614.5(ACTG1):c.985-5T>C rs370546734

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