List of variants in gene ACSF3 reported as uncertain significance for not specified

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001243279.3(ACSF3):c.728C>T (p.Pro243Leu)	rs140986055	0.00022
NM_001243279.3(ACSF3):c.28C>T (p.Arg10Trp)	rs202182978	0.00016
NM_001243279.3(ACSF3):c.1670C>T (p.Pro557Leu)	rs780364085	0.00005
NM_001243279.3(ACSF3):c.828G>T (p.Trp276Cys)	rs570233664	0.00005
NM_001243279.3(ACSF3):c.1470G>C (p.Glu490Asp)	rs147538370	0.00004
NM_001243279.3(ACSF3):c.1721dup (p.His574fs)	rs768886326	0.00004
NM_001243279.3(ACSF3):c.1543C>T (p.Arg515Trp)	rs563580010	0.00002
NM_001243279.3(ACSF3):c.1412G>A (p.Arg471Gln)	rs387907119	0.00001
NC_000016.9:g.(89180896_89187208)_(89212458_89220497)dup
NC_000016.9:g.(?_89160216)_(89187322_89199543)dup
NM_001243279.3(ACSF3):c.1385_1407delinsCGGAT (p.Lys462_Arg469delinsThrAsp)
NM_001243279.3(ACSF3):c.1406G>A (p.Arg469Gln)	rs144681140
NM_001243279.3(ACSF3):c.1673G>A (p.Arg558Gln)	rs140328142
NM_001243279.3(ACSF3):c.311A>T (p.Asn104Ile)	rs1378197369
NM_001243279.3(ACSF3):c.395C>A (p.Ala132Asp)	rs2151407600

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