List of variants in gene GLIS3 reported as likely benign by Invitae

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 94

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HGVS	dbSNP	gnomAD frequency
NM_001042413.2(GLIS3):c.1545G>C (p.Glu515Asp)	rs72687988	0.00304
NM_001042413.2(GLIS3):c.2089G>A (p.Val697Met)	rs148816140	0.00229
NM_001042413.2(GLIS3):c.893C>A (p.Ser298Tyr)	rs148572278	0.00199
NM_001042413.2(GLIS3):c.1191G>C (p.Gln397His)	rs138497710	0.00163
NM_001042413.2(GLIS3):c.496C>G (p.Pro166Ala)	rs141467694	0.00147
NM_001042413.2(GLIS3):c.793G>T (p.Val265Phe)	rs143192828	0.00087
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.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.2421C>G (p.Ser807=)	rs563920093	0.00026
NM_001042413.2(GLIS3):c.422T>C (p.Ile141Thr)	rs202165554	0.00025
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.2538G>A (p.Pro846=)	rs144648063	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.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.2568G>A (p.Ser856=)	rs773065162	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.1071C>T (p.Ser357=)	rs752385722	0.00001
NM_001042413.2(GLIS3):c.1272G>A (p.Ser424=)	rs764287243	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.2297+17C>G	rs747090434	0.00001
NM_001042413.2(GLIS3):c.2657-4C>G	rs777809882	0.00001
NM_001042413.2(GLIS3):c.555A>C (p.Ala185=)	rs752433935	0.00001
NM_001042413.2(GLIS3):c.1035G>A (p.Pro345=)
NM_001042413.2(GLIS3):c.1053C>T (p.Phe351=)	rs1027005598
NM_001042413.2(GLIS3):c.1161C>T (p.Asp387=)
NM_001042413.2(GLIS3):c.1164G>A (p.Gly388=)	rs1586723209
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.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.1830C>T (p.Asn610=)
NM_001042413.2(GLIS3):c.1873-23TTCT[5]
NM_001042413.2(GLIS3):c.1983+19C>T
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.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.2297+11C>G
NM_001042413.2(GLIS3):c.2365C>T (p.Leu789=)
NM_001042413.2(GLIS3):c.2391C>G (p.Thr797=)
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.2484G>T (p.Gly828=)
NM_001042413.2(GLIS3):c.2622C>T (p.Phe874=)
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.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.2784C>T (p.Thr928=)
NM_001042413.2(GLIS3):c.596+9T>A
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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