ClinVar Miner

List of variants in gene GLIS3 reported by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 186
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HGVS dbSNP gnomAD frequency
NM_001042413.2(GLIS3):c.1270T>C (p.Ser424Pro) rs806052 0.99890
NM_001042413.2(GLIS3):c.1367C>A (p.Pro456Gln) rs6415788 0.62075
NM_001042413.2(GLIS3):c.2686C>T (p.Leu896Phe) rs76094493 0.03919
NM_001042413.2(GLIS3):c.1536C>A (p.Asp512Glu) rs148199056 0.01645
NM_001042413.2(GLIS3):c.938G>C (p.Gly313Ala) rs35154632 0.01104
NM_001042413.2(GLIS3):c.171C>T (p.Asn57=) rs117802495 0.00947
NM_001042413.2(GLIS3):c.1216G>T (p.Gly406Cys) rs75462592 0.00898
NM_001042413.2(GLIS3):c.1126C>T (p.Pro376Ser) rs76342955 0.00811
NM_001042413.2(GLIS3):c.1881T>C (p.Tyr627=) rs141985853 0.00500
NM_001042413.2(GLIS3):c.1318A>G (p.Thr440Ala) rs80161424 0.00314
NM_001042413.2(GLIS3):c.1545G>C (p.Glu515Asp) rs72687988 0.00304
NM_001042413.2(GLIS3):c.1117C>G (p.Leu373Val) rs200263979 0.00252
NM_001042413.2(GLIS3):c.2089G>A (p.Val697Met) rs148816140 0.00229
NM_001042413.2(GLIS3):c.1430C>T (p.Ala477Val) rs114838275 0.00207
NM_001042413.2(GLIS3):c.893C>A (p.Ser298Tyr) rs148572278 0.00199
NM_001042413.2(GLIS3):c.232C>G (p.Arg78Gly) rs148168366 0.00178
NM_001042413.2(GLIS3):c.1092G>T (p.Pro364=) rs74680081 0.00172
NM_001042413.2(GLIS3):c.1090C>T (p.Pro364Ser) rs143056249 0.00165
NM_001042413.2(GLIS3):c.954C>T (p.Thr318=) rs75564360 0.00165
NM_001042413.2(GLIS3):c.1191G>C (p.Gln397His) rs138497710 0.00163
NM_001042413.2(GLIS3):c.1767G>T (p.Arg589=) rs138100080 0.00160
NM_001042413.2(GLIS3):c.496C>G (p.Pro166Ala) rs141467694 0.00147
NM_001042413.2(GLIS3):c.1509C>T (p.Arg503=) rs141125402 0.00103
NM_001042413.2(GLIS3):c.793G>T (p.Val265Phe) rs143192828 0.00087
NM_001042413.2(GLIS3):c.1044C>T (p.Tyr348=) rs146238548 0.00086
NM_001042413.2(GLIS3):c.2340G>A (p.Arg780=) rs147473975 0.00086
NM_001042413.2(GLIS3):c.744A>G (p.Leu248=) rs139080385 0.00086
NM_001042413.2(GLIS3):c.1199A>G (p.His400Arg) rs376031632 0.00081
NM_001042413.2(GLIS3):c.1872C>T (p.Thr624=) rs140309338 0.00068
NM_001042413.2(GLIS3):c.2095C>T (p.Arg699Cys) rs145867412 0.00062
NM_001042413.2(GLIS3):c.1452G>A (p.Gln484=) rs143229804 0.00060
NM_001042413.2(GLIS3):c.1260C>T (p.Pro420=) rs377419083 0.00059
NM_001042413.2(GLIS3):c.1788G>A (p.Pro596=) rs150364458 0.00059
NM_001042413.2(GLIS3):c.2709C>T (p.Ser903=) rs137946889 0.00056
NM_001042413.2(GLIS3):c.1873-9C>G rs371770632 0.00036
NM_001042413.2(GLIS3):c.1056G>C (p.Leu352=) rs140880100 0.00029
NM_001042413.2(GLIS3):c.1740G>A (p.Arg580=) rs149545036 0.00029
NM_001042413.2(GLIS3):c.2060C>T (p.Ser687Phe) rs374929970 0.00027
NM_001042413.2(GLIS3):c.1200C>G (p.His400Gln) rs374943049 0.00026
NM_001042413.2(GLIS3):c.2421C>G (p.Ser807=) rs563920093 0.00026
NM_001042413.2(GLIS3):c.422T>C (p.Ile141Thr) rs202165554 0.00025
NM_001042413.2(GLIS3):c.2096G>A (p.Arg699His) rs149840771 0.00023
NM_001042413.2(GLIS3):c.1327C>T (p.Leu443=) rs529418802 0.00022
NM_001042413.2(GLIS3):c.2710G>A (p.Gly904Arg) rs150310830 0.00022
NM_001042413.2(GLIS3):c.1154G>T (p.Gly385Val) rs200959196 0.00019
NM_001042413.2(GLIS3):c.2746G>A (p.Val916Met) rs151140581 0.00019
NM_001042413.2(GLIS3):c.1515C>T (p.Ile505=) rs752036990 0.00016
NM_001042413.2(GLIS3):c.1227C>A (p.Asn409Lys) rs534295783 0.00014
NM_001042413.2(GLIS3):c.2636C>T (p.Ser879Leu) rs200265407 0.00014
NM_001042413.2(GLIS3):c.1994G>A (p.Ser665Asn) rs199817194 0.00011
NM_001042413.2(GLIS3):c.1326C>T (p.Asp442=) rs758928731 0.00010
NM_001042413.2(GLIS3):c.2537C>T (p.Pro846Leu) rs199505727 0.00010
NM_001042413.2(GLIS3):c.2531T>C (p.Ile844Thr) rs193061752 0.00009
NM_001042413.2(GLIS3):c.2538G>A (p.Pro846=) rs144648063 0.00009
NM_001042413.2(GLIS3):c.2753G>A (p.Arg918His) rs147357710 0.00009
NM_001042413.2(GLIS3):c.1984-16C>T rs145670205 0.00008
NM_001042413.2(GLIS3):c.2723C>T (p.Ala908Val) rs140101069 0.00008
NM_001042413.2(GLIS3):c.645G>A (p.Thr215=) rs142323958 0.00008
NM_001042413.2(GLIS3):c.1686T>G (p.Ser562=) rs745836279 0.00007
NM_001042413.2(GLIS3):c.888C>T (p.Ala296=) rs781296682 0.00007
NM_001042413.2(GLIS3):c.2077G>A (p.Ala693Thr) rs568262538 0.00006
NM_001042413.2(GLIS3):c.1368A>T (p.Pro456=) rs755087869 0.00005
NM_001042413.2(GLIS3):c.2297+16T>C rs377104078 0.00005
NM_001042413.2(GLIS3):c.1310C>T (p.Pro437Leu) rs745511715 0.00004
NM_001042413.2(GLIS3):c.1779C>T (p.Gly593=) rs370278575 0.00004
NM_001042413.2(GLIS3):c.1842C>T (p.Arg614=) rs758753292 0.00004
NM_001042413.2(GLIS3):c.2107C>T (p.Pro703Ser) rs200705602 0.00004
NM_001042413.2(GLIS3):c.2258A>G (p.Gln753Arg) rs750346762 0.00004
NM_001042413.2(GLIS3):c.2568G>A (p.Ser856=) rs773065162 0.00004
NM_001042413.2(GLIS3):c.937G>A (p.Gly313Arg) rs368943263 0.00004
NM_001042413.2(GLIS3):c.1263C>T (p.Asp421=) rs755713904 0.00003
NM_001042413.2(GLIS3):c.2283C>T (p.Asp761=) rs202217571 0.00003
NM_001042413.2(GLIS3):c.2681C>T (p.Ser894Leu) rs202168959 0.00002
NM_001042413.2(GLIS3):c.2705G>A (p.Arg902His) rs772126214 0.00002
NM_001042413.2(GLIS3):c.950A>G (p.Asn317Ser) rs201716083 0.00002
NM_001042413.2(GLIS3):c.1071C>T (p.Ser357=) rs752385722 0.00001
NM_001042413.2(GLIS3):c.1210C>A (p.Gln404Lys) rs751660790 0.00001
NM_001042413.2(GLIS3):c.1272G>A (p.Ser424=) rs764287243 0.00001
NM_001042413.2(GLIS3):c.1416G>T (p.Glu472Asp) rs772552747 0.00001
NM_001042413.2(GLIS3):c.1521C>T (p.Cys507=) rs908630522 0.00001
NM_001042413.2(GLIS3):c.1563C>T (p.Ile521=) rs757028972 0.00001
NM_001042413.2(GLIS3):c.1898G>A (p.Gly633Glu) rs757071195 0.00001
NM_001042413.2(GLIS3):c.2297+17C>G rs747090434 0.00001
NM_001042413.2(GLIS3):c.2503C>G (p.Pro835Ala) rs753899353 0.00001
NM_001042413.2(GLIS3):c.2657-4C>G rs777809882 0.00001
NM_001042413.2(GLIS3):c.2669C>A (p.Pro890His) rs1817846206 0.00001
NM_001042413.2(GLIS3):c.555A>C (p.Ala185=) rs752433935 0.00001
NM_001042413.2(GLIS3):c.758G>T (p.Ser253Ile) rs372326856 0.00001
NC_000009.11:g.(?_3828272)_(3829512_?)del
NC_000009.11:g.(?_4117748)_(4125864_?)dup
NM_001042413.2(GLIS3):c.1006G>T (p.Ala336Ser)
NM_001042413.2(GLIS3):c.1013C>T (p.Pro338Leu)
NM_001042413.2(GLIS3):c.1034C>T (p.Pro345Leu)
NM_001042413.2(GLIS3):c.1035G>A (p.Pro345=)
NM_001042413.2(GLIS3):c.1053C>T (p.Phe351=) rs1027005598
NM_001042413.2(GLIS3):c.1073G>T (p.Cys358Phe)
NM_001042413.2(GLIS3):c.1085C>A (p.Pro362Gln) rs146131512
NM_001042413.2(GLIS3):c.1091C>T (p.Pro364Leu)
NM_001042413.2(GLIS3):c.1120G>T (p.Val374Leu)
NM_001042413.2(GLIS3):c.1145C>A (p.Pro382Gln)
NM_001042413.2(GLIS3):c.1149C>G (p.Ala383=) rs763014102
NM_001042413.2(GLIS3):c.1153G>A (p.Gly385Ser)
NM_001042413.2(GLIS3):c.1161C>T (p.Asp387=)
NM_001042413.2(GLIS3):c.1164G>A (p.Gly388=) rs1586723209
NM_001042413.2(GLIS3):c.1233G>C (p.Met411Ile)
NM_001042413.2(GLIS3):c.1300G>A (p.Glu434Lys) rs2130877806
NM_001042413.2(GLIS3):c.1306T>G (p.Phe436Val)
NM_001042413.2(GLIS3):c.1335C>A (p.Pro445=)
NM_001042413.2(GLIS3):c.1335C>G (p.Pro445=)
NM_001042413.2(GLIS3):c.1359G>C (p.Pro453=)
NM_001042413.2(GLIS3):c.1383T>A (p.Pro461=) rs1398641546
NM_001042413.2(GLIS3):c.1417C>T (p.Leu473Phe)
NM_001042413.2(GLIS3):c.1443C>G (p.Ala481=)
NM_001042413.2(GLIS3):c.1446G>A (p.Leu482=)
NM_001042413.2(GLIS3):c.1500T>C (p.His500=)
NM_001042413.2(GLIS3):c.1590A>G (p.Lys530=)
NM_001042413.2(GLIS3):c.1617C>T (p.Ala539=)
NM_001042413.2(GLIS3):c.1653C>A (p.Arg551=)
NM_001042413.2(GLIS3):c.1663C>T (p.Leu555=)
NM_001042413.2(GLIS3):c.1710+16G>A rs142098538
NM_001042413.2(GLIS3):c.1710+16G>T
NM_001042413.2(GLIS3):c.1806G>A (p.Pro602=)
NM_001042413.2(GLIS3):c.1808G>A (p.Gly603Asp)
NM_001042413.2(GLIS3):c.1830C>T (p.Asn610=)
NM_001042413.2(GLIS3):c.1873-23TTCT[5]
NM_001042413.2(GLIS3):c.1909C>T (p.Arg637Cys)
NM_001042413.2(GLIS3):c.1983+19C>T
NM_001042413.2(GLIS3):c.1983+3A>T rs1825674540
NM_001042413.2(GLIS3):c.1983+6T>G
NM_001042413.2(GLIS3):c.1983+9_1983+10insGGAAAAAGGTAATTTTATTTTTTTTTTTTTTTTTTTTNNNNNNNNNNGGTCAGGGGCGCGCTTACGCGGGGAGGCTCCTGTGCTCTCCGGCTGCTGGGGCGACGGGTTTGGGGGGGGGGGGGTTAGCTGGGAGGGGAGAATCCAACAATC
NM_001042413.2(GLIS3):c.1984-17C>T
NM_001042413.2(GLIS3):c.2010A>G (p.Pro670=)
NM_001042413.2(GLIS3):c.2034C>T (p.Thr678=)
NM_001042413.2(GLIS3):c.2086A>C (p.Thr696Pro)
NM_001042413.2(GLIS3):c.2109C>T (p.Pro703=)
NM_001042413.2(GLIS3):c.2128+19G>C
NM_001042413.2(GLIS3):c.2190C>T (p.Pro730=)
NM_001042413.2(GLIS3):c.2208C>T (p.His736=)
NM_001042413.2(GLIS3):c.2244C>A (p.His748Gln)
NM_001042413.2(GLIS3):c.2297+11C>G
NM_001042413.2(GLIS3):c.2297+11_2297+12del rs779433100
NM_001042413.2(GLIS3):c.2328C>G (p.His776Gln)
NM_001042413.2(GLIS3):c.2365C>T (p.Leu789=)
NM_001042413.2(GLIS3):c.2375C>G (p.Thr792Arg)
NM_001042413.2(GLIS3):c.2391C>G (p.Thr797=)
NM_001042413.2(GLIS3):c.2459G>T (p.Gly820Val)
NM_001042413.2(GLIS3):c.2471A>C (p.His824Pro)
NM_001042413.2(GLIS3):c.2471A>G (p.His824Arg) rs140981222
NM_001042413.2(GLIS3):c.2473+12G>A
NM_001042413.2(GLIS3):c.2473+13C>G
NM_001042413.2(GLIS3):c.2473+13C>T rs368773221
NM_001042413.2(GLIS3):c.2474-8C>T
NM_001042413.2(GLIS3):c.2474G>C (p.Gly825Ala)
NM_001042413.2(GLIS3):c.2484G>T (p.Gly828=)
NM_001042413.2(GLIS3):c.2515C>G (p.Pro839Ala)
NM_001042413.2(GLIS3):c.2518G>A (p.Asp840Asn)
NM_001042413.2(GLIS3):c.2571T>G (p.Phe857Leu)
NM_001042413.2(GLIS3):c.2622C>T (p.Phe874=)
NM_001042413.2(GLIS3):c.2636C>G (p.Ser879Trp) rs200265407
NM_001042413.2(GLIS3):c.2637G>T (p.Ser879=)
NM_001042413.2(GLIS3):c.2656+16G>C
NM_001042413.2(GLIS3):c.2656+20C>T
NM_001042413.2(GLIS3):c.2657-17C>T rs746005781
NM_001042413.2(GLIS3):c.2657-8T>C
NM_001042413.2(GLIS3):c.2659T>C (p.Tyr887His)
NM_001042413.2(GLIS3):c.2670T>G (p.Pro890=) rs1588038507
NM_001042413.2(GLIS3):c.2682G>A (p.Ser894=)
NM_001042413.2(GLIS3):c.2688C>T (p.Leu896=)
NM_001042413.2(GLIS3):c.2694G>T (p.Gly898=)
NM_001042413.2(GLIS3):c.2716G>A (p.Glu906Lys) rs1485002019
NM_001042413.2(GLIS3):c.2742C>G (p.Ser914Arg)
NM_001042413.2(GLIS3):c.2767C>T (p.Leu923Phe)
NM_001042413.2(GLIS3):c.2784C>T (p.Thr928=)
NM_001042413.2(GLIS3):c.472G>T (p.Val158Phe)
NM_001042413.2(GLIS3):c.596+9T>A
NM_001042413.2(GLIS3):c.652C>G (p.Gln218Glu)
NM_001042413.2(GLIS3):c.720C>T (p.His240=) rs752839353
NM_001042413.2(GLIS3):c.759C>T (p.Ser253=)
NM_001042413.2(GLIS3):c.771G>C (p.Gly257=)
NM_001042413.2(GLIS3):c.789T>C (p.Asn263=)
NM_001042413.2(GLIS3):c.810A>G (p.Pro270=) rs376404333
NM_001042413.2(GLIS3):c.816C>T (p.Tyr272=)
NM_001042413.2(GLIS3):c.822T>C (p.Phe274=) rs750596069
NM_001042413.2(GLIS3):c.844C>G (p.Pro282Ala) rs143051164
NM_001042413.2(GLIS3):c.993C>T (p.Ile331=)
NM_001042413.2(GLIS3):c.999G>T (p.Gly333=)

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