List of variants in gene ACTG1 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_001614.5(ACTG1):c.780G>A (p.Ala260=)	rs140846345	0.00287
NM_001614.5(ACTG1):c.18C>T (p.Ala6=)	rs145211830	0.00128
NM_001614.5(ACTG1):c.531T>C (p.Arg177=)	rs143851458	0.00106
NM_001614.5(ACTG1):c.774G>A (p.Pro258=)	rs61997068	0.00053
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.345C>T (p.Asn115=)	rs149057480	0.00021
NM_001614.5(ACTG1):c.159C>T (p.Tyr53=)	rs139751304	0.00019
NM_001614.5(ACTG1):c.825C>T (p.His275=)	rs145303691	0.00017
NM_001614.5(ACTG1):c.954C>T (p.Thr318=)	rs3211110	0.00009
NM_001614.5(ACTG1):c.669C>T (p.Phe223=)	rs373099591	0.00008
NM_001614.5(ACTG1):c.168C>T (p.Asp56=)	rs368299537	0.00007
NM_001614.5(ACTG1):c.267C>T (p.Thr89=)	rs140398667	0.00006
NM_001614.5(ACTG1):c.255C>T (p.Ile85=)	rs147001458	0.00004
NM_001614.5(ACTG1):c.803-13C>T	rs376658586	0.00004
NM_001614.5(ACTG1):c.498C>T (p.Tyr166=)	rs373572370	0.00003
NM_001614.5(ACTG1):c.696C>T (p.Ser232=)	rs202155328	0.00003
NM_001614.5(ACTG1):c.909C>T (p.Thr303=)	rs187127467	0.00003
NM_001614.5(ACTG1):c.957C>T (p.Ala319=)	rs377745600	0.00003
NM_001614.5(ACTG1):c.1110C>A (p.Val370=)	rs727502879	0.00002
NM_001614.5(ACTG1):c.945G>A (p.Lys315=)	rs727502881	0.00002
NM_001614.5(ACTG1):c.150G>A (p.Lys50=)	rs1482374138	0.00001
NM_001614.5(ACTG1):c.390G>A (p.Pro130=)	rs561518636	0.00001
NM_001614.5(ACTG1):c.405C>T (p.Ala135=)	rs576214455	0.00001
NM_001614.5(ACTG1):c.636C>A (p.Ile212=)	rs727502883	0.00001
NM_001614.5(ACTG1):c.642G>A (p.Glu214=)	rs782187026	0.00001
NM_001614.5(ACTG1):c.828G>A (p.Glu276=)	rs727504806	0.00001
NM_001614.5(ACTG1):c.1041C>T (p.Ala347=)	rs375903517
NM_001614.5(ACTG1):c.315G>A (p.Leu105=)	rs202094234
NM_001614.5(ACTG1):c.333C>T (p.Asn111=)	rs727502884
NM_001614.5(ACTG1):c.414C>T (p.Ala138=)	rs143978597
NM_001614.5(ACTG1):c.432C>T (p.Ala144=)	rs372748659
NM_001614.5(ACTG1):c.576C>T (p.Ile192=)	rs186443800
NM_001614.5(ACTG1):c.803-7C>T	rs150136833
NM_001614.5(ACTG1):c.985-5dup	rs782289893
NM_001614.5(ACTG1):c.996C>A (p.Pro332=)	rs200089021

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