ClinVar Miner

List of variants in gene DNAAF1 reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_178452.6(DNAAF1):c.1245C>G (p.Thr415=) rs147804813 0.00233
NM_178452.6(DNAAF1):c.113G>C (p.Gly38Ala) rs200992452 0.00086
NM_178452.6(DNAAF1):c.432C>T (p.Ile144=) rs143312655 0.00063
NM_178452.6(DNAAF1):c.1495C>A (p.Pro499Thr) rs201519478 0.00050
NM_178452.6(DNAAF1):c.1299C>T (p.Asp433=) rs141074491 0.00044
NM_178452.6(DNAAF1):c.1506G>A (p.Pro502=) rs373515859 0.00036
NM_178452.6(DNAAF1):c.1350G>A (p.Pro450=) rs148990251 0.00026
NM_178452.6(DNAAF1):c.735C>T (p.Pro245=) rs139566676 0.00023
NM_178452.6(DNAAF1):c.1068C>T (p.Pro356=) rs370118109 0.00021
NM_178452.6(DNAAF1):c.115T>C (p.Cys39Arg) rs373512514 0.00019
NM_178452.6(DNAAF1):c.1377T>A (p.Asp459Glu) rs761136963 0.00014
NM_178452.6(DNAAF1):c.2079C>T (p.Ser693=) rs145469545 0.00011
NM_178452.6(DNAAF1):c.2166G>A (p.Pro722=) rs764624773 0.00011
NM_178452.6(DNAAF1):c.507G>C (p.Leu169=) rs370128838 0.00011
NM_178452.6(DNAAF1):c.1317G>A (p.Glu439=) rs768024430 0.00009
NM_178452.6(DNAAF1):c.1735T>C (p.Leu579=) rs764511452 0.00009
NM_178452.6(DNAAF1):c.2080G>A (p.Ala694Thr) rs376164700 0.00007
NM_178452.6(DNAAF1):c.768G>A (p.Pro256=) rs142601761 0.00006
NM_178452.6(DNAAF1):c.1423C>T (p.Leu475=) rs368651695 0.00005
NM_178452.6(DNAAF1):c.1592C>T (p.Thr531Met) rs193291760 0.00005
NM_178452.6(DNAAF1):c.1593G>A (p.Thr531=) rs372197911 0.00004
NM_178452.6(DNAAF1):c.1587G>A (p.Thr529=) rs769031288 0.00003
NM_178452.6(DNAAF1):c.315C>G (p.Thr105=) rs144962513 0.00003
NM_178452.6(DNAAF1):c.2070G>A (p.Pro690=) rs772036783 0.00001
NM_178452.6(DNAAF1):c.705G>A (p.Pro235=) rs759831401 0.00001
NM_178452.6(DNAAF1):c.1007G>A (p.Arg336Lys)
NM_178452.6(DNAAF1):c.107G>C (p.Arg36Pro)
NM_178452.6(DNAAF1):c.1098C>G (p.Pro366=)
NM_178452.6(DNAAF1):c.1131A>G (p.Leu377=)
NM_178452.6(DNAAF1):c.1161C>T (p.Asp387=)
NM_178452.6(DNAAF1):c.1167C>G (p.Leu389=)
NM_178452.6(DNAAF1):c.1182A>G (p.Pro394=)
NM_178452.6(DNAAF1):c.1356T>A (p.Pro452=)
NM_178452.6(DNAAF1):c.1377T>C (p.Asp459=) rs761136963
NM_178452.6(DNAAF1):c.13C>G (p.Pro5Ala)
NM_178452.6(DNAAF1):c.1416C>T (p.Thr472=)
NM_178452.6(DNAAF1):c.1529-17TTG[2] rs369485504
NM_178452.6(DNAAF1):c.155G>A (p.Gly52Asp)
NM_178452.6(DNAAF1):c.1614A>G (p.Arg538=)
NM_178452.6(DNAAF1):c.1740T>C (p.Ser580=)
NM_178452.6(DNAAF1):c.1770G>A (p.Thr590=)
NM_178452.6(DNAAF1):c.1780G>A (p.Val594Met)
NM_178452.6(DNAAF1):c.1798A>G (p.Thr600Ala)
NM_178452.6(DNAAF1):c.1806T>C (p.Thr602=)
NM_178452.6(DNAAF1):c.1807C>T (p.Leu603=)
NM_178452.6(DNAAF1):c.181C>G (p.Gln61Glu) rs886052366
NM_178452.6(DNAAF1):c.1883A>C (p.Glu628Ala)
NM_178452.6(DNAAF1):c.1897T>C (p.Leu633=)
NM_178452.6(DNAAF1):c.1998A>G (p.Gln666=)
NM_178452.6(DNAAF1):c.2019T>C (p.Thr673=)
NM_178452.6(DNAAF1):c.2165C>T (p.Pro722Leu)
NM_178452.6(DNAAF1):c.222C>T (p.Phe74=)
NM_178452.6(DNAAF1):c.327T>C (p.Asn109=)
NM_178452.6(DNAAF1):c.33T>C (p.Gly11=)
NM_178452.6(DNAAF1):c.491G>A (p.Arg164His)
NM_178452.6(DNAAF1):c.663G>A (p.Arg221=)
NM_178452.6(DNAAF1):c.690C>T (p.Asn230=)
NM_178452.6(DNAAF1):c.873G>A (p.Ala291=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.