ClinVar Miner

List of variants in gene GLIS3 reported by Fulgent Genetics, Fulgent Genetics

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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_001042413.2(GLIS3):c.938G>C (p.Gly313Ala) rs35154632 0.01104
NM_001042413.2(GLIS3):c.1318A>G (p.Thr440Ala) rs80161424 0.00314
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.1260C>T (p.Pro420=) rs377419083 0.00059
NM_001042413.2(GLIS3):c.287C>T (p.Pro96Leu) rs143425492 0.00043
NM_001042413.2(GLIS3):c.2060C>T (p.Ser687Phe) rs374929970 0.00027
NM_001042413.2(GLIS3):c.2421C>G (p.Ser807=) rs563920093 0.00026
NM_001042413.2(GLIS3):c.82A>G (p.Ile28Val) rs113754532 0.00026
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.1330C>T (p.Pro444Ser) rs755318788 0.00016
NM_001042413.2(GLIS3):c.275C>T (p.Thr92Ile) rs375931960 0.00015
NM_001042413.2(GLIS3):c.1227C>A (p.Asn409Lys) rs534295783 0.00014
NM_001042413.2(GLIS3):c.2339G>A (p.Arg780Gln) rs200694226 0.00013
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.24G>T (p.Met8Ile) rs201804281 0.00009
NM_001042413.2(GLIS3):c.2531T>C (p.Ile844Thr) rs193061752 0.00009
NM_001042413.2(GLIS3):c.1984-16C>T rs145670205 0.00008
NM_001042413.2(GLIS3):c.1686T>G (p.Ser562=) rs745836279 0.00007
NM_001042413.2(GLIS3):c.1988G>A (p.Arg663Gln) rs144720690 0.00007
NM_001042413.2(GLIS3):c.2027G>T (p.Cys676Phe) rs149983395 0.00007
NM_001042413.2(GLIS3):c.1395T>C (p.His465=) rs752606768 0.00006
NM_001042413.2(GLIS3):c.2494A>G (p.Lys832Glu) rs779354091 0.00006
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.2107C>T (p.Pro703Ser) rs200705602 0.00004
NM_001042413.2(GLIS3):c.1214C>T (p.Pro405Leu) rs764072714 0.00003
NM_001042413.2(GLIS3):c.1263C>T (p.Asp421=) rs755713904 0.00003
NM_001042413.2(GLIS3):c.638G>A (p.Ser213Asn) rs748030278 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.94C>T (p.Arg32Ter) rs753993867 0.00002
NM_001042413.2(GLIS3):c.950A>G (p.Asn317Ser) rs201716083 0.00002
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.220G>A (p.Val74Met) rs768657630 0.00001
NM_001042413.2(GLIS3):c.2350G>C (p.Ala784Pro) rs754312328 0.00001
NM_001042413.2(GLIS3):c.2503C>G (p.Pro835Ala) rs753899353 0.00001
NM_001042413.2(GLIS3):c.555A>C (p.Ala185=) rs752433935 0.00001
NM_001042413.2(GLIS3):c.596+6A>C rs772180668 0.00001
NM_001042413.2(GLIS3):c.*69T>C rs913597564
NM_001042413.2(GLIS3):c.2323C>T (p.His775Tyr) rs745671153
NM_001042413.2(GLIS3):c.2473+13C>T rs368773221
NM_001042413.2(GLIS3):c.2657-17C>T rs746005781
NM_001042413.2(GLIS3):c.388G>A (p.Gly130Arg) rs777378754
NM_001042413.2(GLIS3):c.41C>G (p.Ser14Trp) rs765421766
NM_001042413.2(GLIS3):c.571_572dup (p.Leu191_Asn192insTer) rs1586744173
NM_001042413.2(GLIS3):c.95G>C (p.Arg32Pro) rs375834888

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