List of variants in gene ACSF3 reported as likely benign for not provided

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001243279.3(ACSF3):c.854C>T (p.Pro285Leu)	rs143793502	0.09373
NM_001243279.3(ACSF3):c.1240-22C>T	rs118065221	0.01069
NM_001243279.3(ACSF3):c.1240-130C>T	rs73254074	0.00918
NM_001243279.3(ACSF3):c.-194+84T>A	rs142287889	0.00917
NM_001243279.3(ACSF3):c.666+52G>A	rs61729363	0.00835
NM_001243279.3(ACSF3):c.1367-67C>T	rs187721910	0.00724
NM_001243279.3(ACSF3):c.1240-199G>A	rs72817489	0.00696
NM_001243279.3(ACSF3):c.822+22C>T	rs76192225	0.00501
NM_001243279.3(ACSF3):c.1501+41G>A	rs188828813	0.00488
NM_001243279.3(ACSF3):c.-193-5G>C	rs144570053	0.00485
NM_001243279.3(ACSF3):c.1613+12T>G	rs1430683913	0.00466
NM_001243279.3(ACSF3):c.1614-118G>A	rs113364969	0.00418
NM_001243279.3(ACSF3):c.600C>G (p.Ile200Met)	rs147597284	0.00391
NM_001243279.3(ACSF3):c.1467G>C (p.Val489=)	rs115776284	0.00242
NM_001243279.3(ACSF3):c.822+18C>T	rs370191947	0.00132
NM_001243279.3(ACSF3):c.-187C>T	rs577925407	0.00055
NM_001243279.3(ACSF3):c.756C>T (p.Asn252=)	rs147718091	0.00029
NM_001243279.3(ACSF3):c.-20-6C>G	rs763583313	0.00016
NM_001243279.3(ACSF3):c.285G>A (p.Glu95=)	rs187962814	0.00015
NM_001243279.3(ACSF3):c.312C>T (p.Asn104=)	rs749994320	0.00010
NM_001243279.3(ACSF3):c.-36C>T	rs1466896036	0.00003
NM_001243279.3(ACSF3):c.357C>T (p.Gly119=)	rs182147718	0.00001
NM_001243279.3(ACSF3):c.*66G>T	rs146927450
NM_001243279.3(ACSF3):c.-194+57G>A	rs552196056
NM_001243279.3(ACSF3):c.-30C>G	rs548417953
NM_001243279.3(ACSF3):c.1239+81C>T	rs146927532
NM_001243279.3(ACSF3):c.1406G>A (p.Arg469Gln)	rs144681140
NM_001243279.3(ACSF3):c.36G>T (p.Leu12=)
NM_001243279.3(ACSF3):c.753C>G (p.Val251=)	rs1597898632

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