ClinVar Miner

List of variants in gene HOGA1 reported by Clinical Biochemistry Laboratory, Health Services Laboratory

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 86
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_138413.4(HOGA1):c.912C>A (p.Ala304=) rs12261752 0.29673
NM_138413.4(HOGA1):c.212-21A>G rs11817730 0.19877
NM_138413.4(HOGA1):c.700+67G>A rs2297643 0.16278
NM_138413.4(HOGA1):c.469-25C>T rs7078003 0.14530
NM_138413.4(HOGA1):c.469-31C>T rs75929214 0.09102
NM_138413.4(HOGA1):c.396G>A (p.Ala132=) rs41290456 0.02716
NM_138413.4(HOGA1):c.834+42G>T rs115279832 0.01504
NM_138413.4(HOGA1):c.700+5G>T rs185803104 0.00156
NM_138413.4(HOGA1):c.701-18G>C rs201596675 0.00034
NM_138413.4(HOGA1):c.107C>T (p.Ala36Val) rs201803986 0.00016
NM_138413.4(HOGA1):c.860G>T (p.Gly287Val) rs138207257 0.00009
NM_138413.4(HOGA1):c.569C>T (p.Pro190Leu) rs202047589 0.00007
NM_138413.4(HOGA1):c.834G>A (p.Ala278=) rs770050262 0.00006
NM_138413.4(HOGA1):c.811C>T (p.Arg271Cys) rs367741588 0.00005
NM_138413.4(HOGA1):c.745C>G (p.Gln249Glu) rs368276974 0.00004
NM_138413.4(HOGA1):c.769T>G (p.Cys257Gly) rs267606764 0.00004
NM_138413.4(HOGA1):c.763C>T (p.Arg255Ter) rs796052086 0.00003
NM_138413.4(HOGA1):c.907C>T (p.Arg303Cys) rs149150736 0.00003
NM_138413.4(HOGA1):c.953G>A (p.Arg318His) rs201347931 0.00003
NM_138413.4(HOGA1):c.208C>T (p.Arg70Ter) rs758304537 0.00002
NM_138413.4(HOGA1):c.289C>T (p.Arg97Cys) rs267606762 0.00002
NM_138413.4(HOGA1):c.117C>A (p.Tyr39Ter) rs746419489 0.00001
NM_138413.4(HOGA1):c.209G>C (p.Arg70Pro) rs267606763 0.00001
NM_138413.4(HOGA1):c.221T>G (p.Val74Gly) rs796052084 0.00001
NM_138413.4(HOGA1):c.290G>A (p.Arg97His) rs752252343 0.00001
NM_138413.4(HOGA1):c.529G>T (p.Asp177Tyr) rs777601935 0.00001
NM_138413.4(HOGA1):c.634A>G (p.Thr212Ala) rs779492256 0.00001
NM_138413.4(HOGA1):c.839C>T (p.Thr280Ile) rs756489804 0.00001
NM_138413.4(HOGA1):c.973G>A (p.Gly325Ser) rs777046879 0.00001
NM_138413.4(HOGA1):c.103A>G (p.Ile35Val)
NM_138413.4(HOGA1):c.110G>A (p.Gly37Asp)
NM_138413.4(HOGA1):c.110G>T (p.Gly37Val) rs772722925
NM_138413.4(HOGA1):c.122_123del (p.Pro41fs) rs1564753668
NM_138413.4(HOGA1):c.122del (p.Pro41fs)
NM_138413.4(HOGA1):c.134C>G (p.Pro45Arg) rs764396564
NM_138413.4(HOGA1):c.134C>T (p.Pro45Leu) rs764396564
NM_138413.4(HOGA1):c.158del (p.Asp53fs) rs796052091
NM_138413.4(HOGA1):c.186_187del (p.His62fs)
NM_138413.4(HOGA1):c.189del (p.Lys63fs) rs1247079002
NM_138413.4(HOGA1):c.206T>G (p.Phe69Cys)
NM_138413.4(HOGA1):c.20G>C (p.Trp7Ser)
NM_138413.4(HOGA1):c.212-1G>A
NM_138413.4(HOGA1):c.227G>A (p.Gly76Asp) rs796052088
NM_138413.4(HOGA1):c.238G>T (p.Glu80Ter)
NM_138413.4(HOGA1):c.250del (p.Phe83_Leu84insTer)
NM_138413.4(HOGA1):c.251T>C (p.Leu84Pro)
NM_138413.4(HOGA1):c.266G>A (p.Arg89His)
NM_138413.4(HOGA1):c.308A>T (p.Asn103Ile) rs796052089
NM_138413.4(HOGA1):c.337G>A (p.Glu113Lys) rs150702945
NM_138413.4(HOGA1):c.340+1G>A
NM_138413.4(HOGA1):c.341-82del rs796052083
NM_138413.4(HOGA1):c.346C>T (p.Gln116Ter) rs767405535
NM_138413.4(HOGA1):c.356T>A (p.Val119Glu)
NM_138413.4(HOGA1):c.356T>G (p.Val119Gly)
NM_138413.4(HOGA1):c.376G>A (p.Ala126Thr)
NM_138413.4(HOGA1):c.3G>A (p.Met1Ile)
NM_138413.4(HOGA1):c.41T>A (p.Leu14Gln)
NM_138413.4(HOGA1):c.469-13C>T rs750664684
NM_138413.4(HOGA1):c.469-1G>C
NM_138413.4(HOGA1):c.533T>C (p.Leu178Pro) rs796052090
NM_138413.4(HOGA1):c.535C>A (p.Pro179Thr) rs374327791
NM_138413.4(HOGA1):c.580G>A (p.Gly194Ser)
NM_138413.4(HOGA1):c.634A>C (p.Thr212Pro)
NM_138413.4(HOGA1):c.651dup (p.Gln218fs)
NM_138413.4(HOGA1):c.661G>C (p.Ala221Pro)
NM_138413.4(HOGA1):c.700+2T>A
NM_138413.4(HOGA1):c.720C>A (p.Cys240Ter)
NM_138413.4(HOGA1):c.728C>A (p.Ala243Asp) rs796052085
NM_138413.4(HOGA1):c.733G>A (p.Val245Ile) rs755562733
NM_138413.4(HOGA1):c.743del (p.Ala248fs)
NM_138413.4(HOGA1):c.754C>T (p.Gln252Ter)
NM_138413.4(HOGA1):c.785G>A (p.Trp262Ter)
NM_138413.4(HOGA1):c.787G>T (p.Glu263Ter)
NM_138413.4(HOGA1):c.803_805del (p.Leu268del) rs796052092
NM_138413.4(HOGA1):c.814C>G (p.Leu272Val)
NM_138413.4(HOGA1):c.833C>A (p.Ala278Glu)
NM_138413.4(HOGA1):c.844C>T (p.Arg282Cys)
NM_138413.4(HOGA1):c.845G>A (p.Arg282His)
NM_138413.4(HOGA1):c.85G>T (p.Glu29Ter)
NM_138413.4(HOGA1):c.860G>A (p.Gly287Glu)
NM_138413.4(HOGA1):c.875T>C (p.Met292Thr) rs796052087
NM_138413.4(HOGA1):c.881G>A (p.Trp294Ter)
NM_138413.4(HOGA1):c.895G>C (p.Gly299Arg)
NM_138413.4(HOGA1):c.908G>A (p.Arg303His)
NM_138413.4(HOGA1):c.938AGG[2] (p.Glu315del) rs397509360
NM_138413.4(HOGA1):c.940G>T (p.Glu314Ter)

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.