List of variants in gene ACTG2 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001615.4(ACTG2):c.255+210C>A	rs768290597	0.00012
NM_001615.4(ACTG2):c.118C>T (p.Arg40Cys)	rs587777385
NM_001615.4(ACTG2):c.119G>A (p.Arg40His)	rs587777386
NM_001615.4(ACTG2):c.188G>A (p.Arg63Gln)	rs1573462811
NM_001615.4(ACTG2):c.400T>A (p.Tyr134Asn)	rs587777388
NM_001615.4(ACTG2):c.442C>A (p.Arg148Ser)	rs587777383
NM_001615.4(ACTG2):c.443G>T (p.Arg148Leu)	rs730880256
NM_001615.4(ACTG2):c.532C>T (p.Arg178Cys)	rs78001248
NM_001615.4(ACTG2):c.533G>A (p.Arg178His)	rs587777384
NM_001615.4(ACTG2):c.533G>T (p.Arg178Leu)	rs587777384
NM_001615.4(ACTG2):c.584C>T (p.Thr195Ile)	rs1057520694
NM_001615.4(ACTG2):c.769C>T (p.Arg257Cys)	rs587777387
NM_001615.4(ACTG2):c.770G>A (p.Arg257His)	rs797044959

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