ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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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.1131C>T (p.Ser377=) rs138395741 0.00346
NM_001243279.3(ACSF3):c.852G>A (p.Thr284=) rs183159791 0.00242
NM_001243279.3(ACSF3):c.411C>T (p.Val137=) rs148969539 0.00083
NM_001243279.3(ACSF3):c.1614-10G>C rs370941606 0.00056
NM_001243279.3(ACSF3):c.1614-6C>T rs368789945 0.00046
NM_001243279.3(ACSF3):c.1629G>A (p.Pro543=) rs146779456 0.00034
NM_001243279.3(ACSF3):c.327C>T (p.Val109=) rs141517318 0.00031
NM_001243279.3(ACSF3):c.756C>T (p.Asn252=) rs147718091 0.00029
NM_001243279.3(ACSF3):c.-22G>C rs575978814 0.00013
NM_001243279.3(ACSF3):c.1502-18C>G rs759372180 0.00012
NM_001243279.3(ACSF3):c.258C>T (p.Cys86=) rs560101290 0.00006
NM_001243279.3(ACSF3):c.1501+11G>A rs770771724 0.00003
NM_001243279.3(ACSF3):c.1502-5C>T rs577763495 0.00003
NM_001243279.3(ACSF3):c.1266G>A (p.Glu422=) rs150322170 0.00002
NM_001243279.3(ACSF3):c.1239+9C>G rs376238513 0.00001
NM_001243279.3(ACSF3):c.584A>G (p.Lys195Arg) rs796051921 0.00001
NM_001243279.3(ACSF3):c.666+20G>A rs557738566 0.00001
NM_001243279.3(ACSF3):c.-15C>G rs115469156
NM_001243279.3(ACSF3):c.-20-11C>A rs770106565
NM_001243279.3(ACSF3):c.-29G>C rs148444044
NM_001243279.3(ACSF3):c.-30C>A rs548417953
NM_001243279.3(ACSF3):c.60G>T (p.Arg20=) rs1555560476

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