ClinVar Miner

List of variants in gene ACTG1 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
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.1017G>C (p.Val339=) rs111305526 0.00053
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.654C>T (p.Tyr218=) rs182162229 0.00024
NM_001614.5(ACTG1):c.825C>T (p.His275=) rs145303691 0.00017
NM_001614.5(ACTG1):c.978G>A (p.Lys326=) rs139339869 0.00016
NM_001614.5(ACTG1):c.687C>T (p.Thr229=) rs201036516 0.00011
NM_001614.5(ACTG1):c.984+7C>T rs369691985 0.00011
NM_001614.5(ACTG1):c.1086C>T (p.Tyr362=) rs144114953 0.00009
NM_001614.5(ACTG1):c.612C>T (p.Ala204=) rs368022367 0.00009
NM_001614.5(ACTG1):c.486G>A (p.Thr162=) rs782442814 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.165C>T (p.Gly55=) rs146402466 0.00006
NM_001614.5(ACTG1):c.318C>T (p.Thr106=) rs372370199 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.735C>T (p.Gly245=) rs186289501 0.00005
NM_001614.5(ACTG1):c.363+9C>T rs200000684 0.00004
NM_001614.5(ACTG1):c.138C>T (p.Gly46=) rs374907377 0.00001
NM_001614.5(ACTG1):c.208C>T (p.Pro70Ser) rs1568062708 0.00001
NM_001614.5(ACTG1):c.1041C>T (p.Ala347=) rs375903517
NM_001614.5(ACTG1):c.1119A>G (p.Lys373=)
NM_001614.5(ACTG1):c.123+8G>C
NM_001614.5(ACTG1):c.20C>T (p.Ala7Val)
NM_001614.5(ACTG1):c.276C>T (p.Asn92=)
NM_001614.5(ACTG1):c.363+10G>T
NM_001614.5(ACTG1):c.366T>C (p.Ile122=)
NM_001614.5(ACTG1):c.414C>T (p.Ala138=) rs143978597
NM_001614.5(ACTG1):c.558C>G (p.Thr186=) rs142893042
NM_001614.5(ACTG1):c.558C>T (p.Thr186=) rs142893042
NM_001614.5(ACTG1):c.615G>A (p.Glu205=)
NM_001614.5(ACTG1):c.630C>T (p.Arg210=)
NM_001614.5(ACTG1):c.655G>A (p.Val219Ile) rs2143777781
NM_001614.5(ACTG1):c.674A>G (p.Gln225Arg)
NM_001614.5(ACTG1):c.802+7G>A
NM_001614.5(ACTG1):c.803-7C>T rs150136833
NM_001614.5(ACTG1):c.876C>T (p.Asp292=)
NM_001614.5(ACTG1):c.948G>C (p.Glu316Asp)
NM_001614.5(ACTG1):c.984+8G>A
NM_001614.5(ACTG1):c.985-5dup rs782289893
NM_001614.5(ACTG1):c.985-8C>T
NM_001614.5(ACTG1):c.985-9T>G
NM_001614.5(ACTG1):c.998C>G (p.Pro333Arg)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.