ClinVar Miner

List of variants in gene ACSF3 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
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.1131C>T (p.Ser377=) rs138395741 0.00346
NM_001243279.3(ACSF3):c.1467G>C (p.Val489=) rs115776284 0.00242
NM_001243279.3(ACSF3):c.852G>A (p.Thr284=) rs183159791 0.00242
NM_001243279.3(ACSF3):c.822+18C>T rs370191947 0.00132
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.-187C>T rs577925407 0.00055
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.-20-6C>G rs763583313 0.00016
NM_001243279.3(ACSF3):c.285G>A (p.Glu95=) rs187962814 0.00015
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.-36C>T rs1466896036 0.00003
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.357C>T (p.Gly119=) rs182147718 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.*66G>T rs146927450
NM_001243279.3(ACSF3):c.-15C>G rs115469156
NM_001243279.3(ACSF3):c.-194+57G>A rs552196056
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.-30C>G rs548417953
NM_001243279.3(ACSF3):c.1239+81C>T rs146927532
NM_001243279.3(ACSF3):c.60G>T (p.Arg20=) rs1555560476

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