ClinVar Miner

List of variants in gene HOGA1 studied for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 103
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HGVS dbSNP
HOGA1, IVS, G-T, +4
NM_138413.3:c.10_11ins5 rs924232072
NM_138413.4(HOGA1):c.*101C>T rs41290458
NM_138413.4(HOGA1):c.*1047T>C rs537101942
NM_138413.4(HOGA1):c.*1059A>C rs886047524
NM_138413.4(HOGA1):c.*186C>A rs576078709
NM_138413.4(HOGA1):c.*186C>T rs576078709
NM_138413.4(HOGA1):c.*204T>A rs886047519
NM_138413.4(HOGA1):c.*288A>C rs886047520
NM_138413.4(HOGA1):c.*289C>T rs540860054
NM_138413.4(HOGA1):c.*290G>A rs144890621
NM_138413.4(HOGA1):c.*292C>T rs771988623
NM_138413.4(HOGA1):c.*313A>C rs933057
NM_138413.4(HOGA1):c.*350dup rs1554875325
NM_138413.4(HOGA1):c.*352T>C rs545072905
NM_138413.4(HOGA1):c.*353_*354dup rs5787248
NM_138413.4(HOGA1):c.*354dup rs5787248
NM_138413.4(HOGA1):c.*355C>T rs1977642
NM_138413.4(HOGA1):c.*359dup rs561998392
NM_138413.4(HOGA1):c.*381_*382AG[1] rs886047523
NM_138413.4(HOGA1):c.*425T>C rs189957405
NM_138413.4(HOGA1):c.*445A>G rs1812286
NM_138413.4(HOGA1):c.*485C>T rs553100036
NM_138413.4(HOGA1):c.*498G>A rs2018017
NM_138413.4(HOGA1):c.*560T>C rs1977641
NM_138413.4(HOGA1):c.*637G>A rs1977640
NM_138413.4(HOGA1):c.*711G>A rs11189295
NM_138413.4(HOGA1):c.*733C>T rs764120248
NM_138413.4(HOGA1):c.*850G>T rs560555907
NM_138413.4(HOGA1):c.*950G>A rs190392004
NM_138413.4(HOGA1):c.-279G>A rs41309988
NM_138413.4(HOGA1):c.107C>T (p.Ala36Val) rs201803986
NM_138413.4(HOGA1):c.110G>T (p.Gly37Val) rs772722925
NM_138413.4(HOGA1):c.117C>A (p.Tyr39Ter) rs746419489
NM_138413.4(HOGA1):c.122dup (p.Val42fs) rs1425736036
NM_138413.4(HOGA1):c.123del (p.Pro41_Val42insTer) rs1419840309
NM_138413.4(HOGA1):c.134C>T (p.Pro45Leu) rs764396564
NM_138413.4(HOGA1):c.158del (p.Asp53fs) rs796052091
NM_138413.4(HOGA1):c.185A>T (p.His62Leu) rs150812556
NM_138413.4(HOGA1):c.208C>T (p.Arg70Ter) rs758304537
NM_138413.4(HOGA1):c.209G>C (p.Arg70Pro) rs267606763
NM_138413.4(HOGA1):c.212-21A>G rs11817730
NM_138413.4(HOGA1):c.212-6T>C rs372066473
NM_138413.4(HOGA1):c.221T>G (p.Val74Gly) rs796052084
NM_138413.4(HOGA1):c.227G>A (p.Gly76Asp) rs796052088
NM_138413.4(HOGA1):c.22_24TCT[1] (p.Ser9del) rs1554872338
NM_138413.4(HOGA1):c.289C>T (p.Arg97Cys) rs267606762
NM_138413.4(HOGA1):c.308A>T (p.Asn103Ile) rs796052089
NM_138413.4(HOGA1):c.331G>A (p.Gly111Arg) rs200529020
NM_138413.4(HOGA1):c.337G>A (p.Glu113Lys) rs150702945
NM_138413.4(HOGA1):c.341-1G>A rs1554874130
NM_138413.4(HOGA1):c.341-82del rs796052083
NM_138413.4(HOGA1):c.346C>T (p.Gln116Ter) rs767405535
NM_138413.4(HOGA1):c.396G>A (p.Ala132=) rs41290456
NM_138413.4(HOGA1):c.398C>T (p.Ala133Val) rs374367160
NM_138413.4(HOGA1):c.39G>A (p.Gly13=) rs200127255
NM_138413.4(HOGA1):c.404del (p.Val135fs) rs1554874148
NM_138413.4(HOGA1):c.413del (p.Pro138fs) rs777683624
NM_138413.4(HOGA1):c.448del (p.Leu150fs) rs746776892
NM_138413.4(HOGA1):c.469-13C>T rs750664684
NM_138413.4(HOGA1):c.469-25C>T rs7078003
NM_138413.4(HOGA1):c.469-31C>T rs75929214
NM_138413.4(HOGA1):c.529G>T (p.Asp177Tyr) rs777601935
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.538G>A (p.Val180Met) rs114177505
NM_138413.4(HOGA1):c.569C>T (p.Pro190Leu) rs202047589
NM_138413.4(HOGA1):c.634A>G (p.Thr212Ala) rs779492256
NM_138413.4(HOGA1):c.700+2T>G rs990830655
NM_138413.4(HOGA1):c.700+5G>T rs185803104
NM_138413.4(HOGA1):c.700+67G>A rs2297643
NM_138413.4(HOGA1):c.700+7C>T rs57616820
NM_138413.4(HOGA1):c.700+9C>T rs375091787
NM_138413.4(HOGA1):c.701-11_701-8dup rs143018385
NM_138413.4(HOGA1):c.701-18G>C rs201596675
NM_138413.4(HOGA1):c.701-2A>G rs776817346
NM_138413.4(HOGA1):c.713del (p.Gly238fs) rs760930050
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.745C>G (p.Gln249Glu) rs368276974
NM_138413.4(HOGA1):c.752G>C (p.Cys251Ser) rs886047518
NM_138413.4(HOGA1):c.763C>T (p.Arg255Ter) rs796052086
NM_138413.4(HOGA1):c.769T>G (p.Cys257Gly) rs267606764
NM_138413.4(HOGA1):c.777G>A (p.Thr259=) rs34820265
NM_138413.4(HOGA1):c.796C>T (p.Gln266Ter) rs752277936
NM_138413.4(HOGA1):c.803_805del (p.Leu268del) rs796052092
NM_138413.4(HOGA1):c.828C>T (p.Asn276=) rs201683794
NM_138413.4(HOGA1):c.834+1G>A rs749315029
NM_138413.4(HOGA1):c.834+1G>T rs749315029
NM_138413.4(HOGA1):c.834+42G>T rs115279832
NM_138413.4(HOGA1):c.834G>A (p.Ala278=) rs770050262
NM_138413.4(HOGA1):c.834_834+1delinsTT rs1564760008
NM_138413.4(HOGA1):c.839C>T (p.Thr280Ile) rs756489804
NM_138413.4(HOGA1):c.860G>T (p.Gly287Val) rs138207257
NM_138413.4(HOGA1):c.872T>C (p.Ile291Thr) rs1554875257
NM_138413.4(HOGA1):c.875T>C (p.Met292Thr) rs796052087
NM_138413.4(HOGA1):c.907C>T (p.Arg303Cys) rs149150736
NM_138413.4(HOGA1):c.910G>A (p.Ala304Thr) rs116527624
NM_138413.4(HOGA1):c.912C>A (p.Ala304=) rs12261752
NM_138413.4(HOGA1):c.91_93AAG[1] (p.Lys32del) rs750736378
NM_138413.4(HOGA1):c.938_940AGG[2] (p.Glu315del) rs397509360
NM_138413.4(HOGA1):c.943_954dup (p.Glu315_Arg318dup) rs777828182
NM_138413.4(HOGA1):c.973G>A (p.Gly325Ser) rs777046879

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