List of variants in gene JUP reported as likely benign for not specified

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: 91

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HGVS	dbSNP	gnomAD frequency
NM_002230.4(JUP):c.425G>A (p.Arg142His)	rs41283425	0.03910
NM_002230.4(JUP):c.1942G>A (p.Val648Ile)	rs143043662	0.00760
NM_002230.4(JUP):c.1159-13C>A	rs201627219	0.00258
NM_002230.4(JUP):c.567C>T (p.Val189=)	rs35297577	0.00090
NM_002230.4(JUP):c.1054+7A>T	rs371988639	0.00049
NM_002230.4(JUP):c.297G>A (p.Ser99=)	rs200976464	0.00049
NM_002230.4(JUP):c.1366G>A (p.Val456Ile)	rs78437817	0.00036
NM_002230.4(JUP):c.633C>T (p.Asn211=)	rs372145644	0.00036
NM_002230.4(JUP):c.459C>T (p.Asp153=)	rs376289528	0.00029
NM_002230.4(JUP):c.486G>A (p.Ala162=)	rs113317262	0.00026
NM_002230.4(JUP):c.1910G>A (p.Arg637His)	rs142095597	0.00025
NM_002230.4(JUP):c.546G>A (p.Ser182=)	rs202038498	0.00023
NM_002230.4(JUP):c.2207C>T (p.Pro736Leu)	rs151178348	0.00022
NM_002230.4(JUP):c.1507G>A (p.Gly503Ser)	rs376051686	0.00021
NM_002230.4(JUP):c.258G>A (p.Arg86=)	rs147159111	0.00020
NM_002230.4(JUP):c.1377G>T (p.Leu459=)	rs147370522	0.00018
NM_002230.4(JUP):c.2031G>A (p.Pro677=)	rs188888662	0.00018
NM_002230.4(JUP):c.1296C>T (p.Asn432=)	rs544224850	0.00017
NM_002230.4(JUP):c.2178C>T (p.Ile726=)	rs141295561	0.00016
NM_002230.4(JUP):c.2086+13C>T	rs199935213	0.00015
NM_002230.4(JUP):c.708-4C>G	rs201313464	0.00014
NM_002230.4(JUP):c.801C>T (p.Ala267=)	rs138397457	0.00014
NM_002230.4(JUP):c.84G>A (p.Ser28=)	rs144137028	0.00014
NM_002230.4(JUP):c.1365C>T (p.Ala455=)	rs77375949	0.00013
NM_002230.4(JUP):c.545C>T (p.Ser182Leu)	rs145592971	0.00013
NM_002230.4(JUP):c.1959C>T (p.Ser653=)	rs375451560	0.00012
NM_002230.4(JUP):c.1159-20G>A	rs782463183	0.00011
NM_002230.4(JUP):c.1989C>T (p.Arg663=)	rs145175985	0.00011
NM_002230.4(JUP):c.*312G>A	rs552155645	0.00009
NM_002230.4(JUP):c.475G>T (p.Val159Leu)	rs782702266	0.00008
NM_002230.4(JUP):c.891C>T (p.Tyr297=)	rs397517302	0.00008
NM_002230.4(JUP):c.1055-14del	rs140002183	0.00006
NM_002230.4(JUP):c.1713C>G (p.Ala571=)	rs138446862	0.00006
NM_002230.4(JUP):c.1912A>C (p.Asn638His)	rs782658008	0.00006
NM_002230.4(JUP):c.568G>A (p.Val190Met)	rs370143312	0.00006
NM_002230.4(JUP):c.762C>T (p.Leu254=)	rs781805854	0.00006
NM_002230.4(JUP):c.1035G>C (p.Lys345Asn)	rs150194093	0.00004
NM_002230.4(JUP):c.1371C>T (p.Cys457=)	rs531692563	0.00004
NM_002230.4(JUP):c.1914C>T (p.Asn638=)	rs368772249	0.00004
NM_002230.4(JUP):c.1932C>T (p.Tyr644=)	rs201704572	0.00004
NM_002230.4(JUP):c.2086+14G>A	rs727504485	0.00004
NM_002230.4(JUP):c.945C>T (p.Leu315=)	rs146804895	0.00004
NM_002230.4(JUP):c.1218C>T (p.Asn406=)	rs782565128	0.00003
NM_002230.4(JUP):c.1290A>G (p.Thr430=)	rs897549158	0.00003
NM_002230.4(JUP):c.1653+18G>A	rs1057520950	0.00003
NM_002230.4(JUP):c.357G>A (p.Pro119=)	rs782579395	0.00003
NM_002230.4(JUP):c.509C>T (p.Ser170Leu)	rs782284038	0.00003
NM_002230.4(JUP):c.66C>T (p.Tyr22=)	rs782575179	0.00003
NM_002230.4(JUP):c.-4C>T	rs782493861	0.00002
NM_002230.4(JUP):c.1924+18A>C	rs1057520892	0.00002
NM_002230.4(JUP):c.351C>T (p.Ala117=)	rs397517300	0.00002
NM_002230.4(JUP):c.707+14C>T	rs1313165709	0.00002
NM_002230.4(JUP):c.1017C>T (p.Ser339=)	rs782357007	0.00001
NM_002230.4(JUP):c.1128G>A (p.Leu376=)	rs781926392	0.00001
NM_002230.4(JUP):c.1165C>T (p.Leu389=)	rs1057523570	0.00001
NM_002230.4(JUP):c.1327C>T (p.Leu443=)	rs140537908	0.00001
NM_002230.4(JUP):c.1347C>T (p.Asp449=)	rs763261901	0.00001
NM_002230.4(JUP):c.1506C>T (p.Ile502=)	rs372963143	0.00001
NM_002230.4(JUP):c.1551G>A (p.Pro517=)	rs988891105	0.00001
NM_002230.4(JUP):c.1599G>A (p.Lys533=)	rs150699961	0.00001
NM_002230.4(JUP):c.1762C>T (p.Leu588=)	rs781900856	0.00001
NM_002230.4(JUP):c.1851G>A (p.Ala617=)	rs1031612674	0.00001
NM_002230.4(JUP):c.1854C>T (p.Ala618=)	rs782176670	0.00001
NM_002230.4(JUP):c.1908C>T (p.Ser636=)	rs782122765	0.00001
NM_002230.4(JUP):c.1920C>T (p.Gly640=)	rs376699725	0.00001
NM_002230.4(JUP):c.1924+14G>T	rs201959663	0.00001
NM_002230.4(JUP):c.192G>A (p.Gly64=)	rs141237794	0.00001
NM_002230.4(JUP):c.2086+7G>C	rs727504940	0.00001
NM_002230.4(JUP):c.266T>C (p.Met89Thr)	rs542745694	0.00001
NM_002230.4(JUP):c.414G>A (p.Glu138=)	rs370003514	0.00001
NM_002230.4(JUP):c.469-16del	rs782421393	0.00001
NM_002230.4(JUP):c.624C>T (p.Ile208=)	rs566435665	0.00001
NM_002230.4(JUP):c.750G>A (p.Leu250=)	rs148381639	0.00001
NM_002230.4(JUP):c.990C>T (p.Thr330=)	rs1057521340	0.00001
NM_002230.4(JUP):c.*14A>C	rs1057522449
NM_002230.4(JUP):c.-8-8G>T	rs1057521241
NM_002230.4(JUP):c.1159-13C>T	rs201627219
NM_002230.4(JUP):c.1266C>T (p.Asn422=)	rs1057523741
NM_002230.4(JUP):c.1281G>A (p.Thr427=)	rs373544304
NM_002230.4(JUP):c.1497+14G>A	rs371853838
NM_002230.4(JUP):c.1509C>T (p.Gly503=)	rs782445315
NM_002230.4(JUP):c.1619G>A (p.Arg540His)	rs376881608
NM_002230.4(JUP):c.1824G>T (p.Leu608=)	rs376043057
NM_002230.4(JUP):c.2139G>A (p.Pro713=)	rs782165431
NM_002230.4(JUP):c.2220A>G (p.Ala740=)	rs142102308
NM_002230.4(JUP):c.318G>A (p.Val106=)	rs1555605856
NM_002230.4(JUP):c.708-6C>T	rs782704213
NM_002230.4(JUP):c.846C>T (p.Pro282=)	rs782262002
NM_002230.4(JUP):c.879G>A (p.Gln293=)	rs1555604492
NM_002230.4(JUP):c.909+6C>T	rs193922705
NM_002230.4(JUP):c.981G>A (p.Leu327=)	rs1295630627

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