ClinVar Miner

List of variants in gene ACSF3 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_001243279.3(ACSF3):c.51G>C (p.Ala17=) rs7201122 0.91794
NM_001243279.3(ACSF3):c.977+185T>C rs4782329 0.75837
NM_001243279.3(ACSF3):c.-20-238G>A rs12445614 0.74599
NM_001243279.3(ACSF3):c.5T>C (p.Leu2Pro) rs7188200 0.72412
NM_001243279.3(ACSF3):c.-20-129C>T rs7195892 0.72305
NM_001243279.3(ACSF3):c.-20-263A>G rs12449019 0.72281
NM_001243279.3(ACSF3):c.354T>C (p.Ser118=) rs6500528 0.72028
NM_001243279.3(ACSF3):c.342G>C (p.Ala114=) rs6500527 0.72026
NM_001243279.3(ACSF3):c.667-77G>C rs4782458 0.72002
NM_001243279.3(ACSF3):c.667-287A>G rs7194635 0.71995
NM_001243279.3(ACSF3):c.315T>C (p.Asp105=) rs7193255 0.71937
NM_001243279.3(ACSF3):c.369C>A (p.Val123=) rs6500529 0.71928
NM_001243279.3(ACSF3):c.306C>T (p.Cys102=) rs6500526 0.71888
NM_001243279.3(ACSF3):c.822+38C>G rs4782456 0.71783
NM_001243279.3(ACSF3):c.822+145T>C rs4782455 0.71040
NM_001243279.3(ACSF3):c.667-31T>C rs4782457 0.71038
NM_001243279.3(ACSF3):c.667-101T>C rs7200676 0.71025
NM_001243279.3(ACSF3):c.666+37C>T rs8060043 0.70606
NM_001243279.3(ACSF3):c.1239+57G>C rs3743983 0.70590
NM_001243279.3(ACSF3):c.822+53_822+54del rs10578141 0.69831
NM_001243279.3(ACSF3):c.977+119A>G rs4782449 0.68672
NM_001243279.3(ACSF3):c.-194+48A>G rs9938075 0.67893
NM_001243279.3(ACSF3):c.666+199T>C rs7194257 0.67347
NM_001243279.3(ACSF3):c.1347G>A (p.Leu449=) rs12447947 0.24857
NM_001243279.3(ACSF3):c.-193-25C>A rs36099289 0.15162
NM_001243279.3(ACSF3):c.667-289C>T rs71387680 0.11988
NM_001243279.3(ACSF3):c.854C>T (p.Pro285Leu) rs143793502 0.09373
NM_001243279.3(ACSF3):c.666+73C>T rs61729367 0.05813
NM_001243279.3(ACSF3):c.1367-183G>A rs73256070 0.05368
NM_001243279.3(ACSF3):c.1501+210A>G rs72817501 0.04278
NM_001243279.3(ACSF3):c.*231G>A rs1054747 0.04215
NM_001243279.3(ACSF3):c.1367-222G>A rs72817500 0.04215
NM_001243279.3(ACSF3):c.1614-25C>T rs72819316 0.04212
NM_001243279.3(ACSF3):c.1614-338C>G rs74659525 0.04203
NM_001243279.3(ACSF3):c.1127-341C>T rs72817472 0.03850
NM_001243279.3(ACSF3):c.49G>C (p.Ala17Pro) rs11547019 0.03850
NM_001243279.3(ACSF3):c.-20-82G>A rs72817434 0.03828
NM_001243279.3(ACSF3):c.1240-339G>A rs12927059 0.03644
NM_001243279.3(ACSF3):c.*265C>A rs113165822 0.03574
NM_001243279.3(ACSF3):c.667-12C>T rs72817437 0.03381
NM_001243279.3(ACSF3):c.822+117G>A rs72817438 0.03371
NM_001243279.3(ACSF3):c.823-52C>T rs72817452 0.03337
NM_001243279.3(ACSF3):c.*73C>T rs79800328 0.02543
NM_001243279.3(ACSF3):c.1367-13C>G rs140859425 0.02493
NM_001243279.3(ACSF3):c.1614-220T>C rs117117251 0.01996
NM_001243279.3(ACSF3):c.1614-321G>A rs117877906 0.01991
NM_001243279.3(ACSF3):c.297C>T (p.Ser99=) rs59213357 0.01079
NM_001243279.3(ACSF3):c.822+106T>C rs78898590 0.01070
NM_001243279.3(ACSF3):c.667-13T>C rs139367843 0.00923
NM_001243279.3(ACSF3):c.1367-6C>T rs113343336 0.00901
NM_001243279.3(ACSF3):c.-20-21C>A rs145819902 0.00383
NM_001243279.3(ACSF3):c.1134G>A (p.Val378=) rs141088268 0.00369
NM_001243279.3(ACSF3):c.-193-14A>G rs181386231 0.00139
NM_001243279.3(ACSF3):c.-14_-13insCCAGGAGGCTCCCGGGAGC rs11273288
NM_001243279.3(ACSF3):c.1366+220C>G rs111644287
NM_001243279.3(ACSF3):c.1367-195C>T rs11076771
NM_001243279.3(ACSF3):c.1367-264A>T rs142820005
NM_001243279.3(ACSF3):c.1502-11_1502-9del rs147884845
NM_001243279.3(ACSF3):c.1502-146A>G rs4302032
NM_001243279.3(ACSF3):c.1502-64A>T rs60881405
NM_001243279.3(ACSF3):c.666+195G>A rs6500530

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