ClinVar Miner

List of variants in gene LMNA reported as uncertain significance by Color

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 139
Download table as spreadsheet
HGVS dbSNP
NM_005572.4(LMNA):c.1201C>T (p.Arg401Cys) rs61094188
NM_005572.4(LMNA):c.1231G>T (p.Gly411Cys) rs727504852
NM_005572.4(LMNA):c.1234G>C (p.Gly412Arg)
NM_005572.4(LMNA):c.1376A>G (p.Asn459Ser) rs372011095
NM_005572.4(LMNA):c.1445G>A (p.Arg482Gln) rs11575937
NM_005572.4(LMNA):c.1567G>A (p.Gly523Arg) rs201583907
NM_005572.4(LMNA):c.1633C>T (p.Arg545Cys) rs267607613
NM_005572.4(LMNA):c.1634G>A (p.Arg545His) rs142191737
NM_005572.4(LMNA):c.1660G>A (p.Glu554Lys)
NM_005572.4(LMNA):c.1664A>G (p.Asp555Gly)
NM_005572.4(LMNA):c.350A>G (p.Lys117Arg) rs397517901
NM_005572.4(LMNA):c.497G>A (p.Arg166Gln) rs267607570
NM_005572.4(LMNA):c.749C>T (p.Ala250Val) rs397517907
NM_005572.4(LMNA):c.976T>A (p.Ser326Thr) rs56851164
NM_170707.4(LMNA):c.*5G>A
NM_170707.4(LMNA):c.-1C>A rs886043355
NM_170707.4(LMNA):c.-4G>A
NM_170707.4(LMNA):c.1001G>A (p.Ser334Asn) rs370656306
NM_170707.4(LMNA):c.1004G>A (p.Arg335Gln) rs138592977
NM_170707.4(LMNA):c.1006C>T (p.Arg336Trp)
NM_170707.4(LMNA):c.1027C>T (p.Arg343Trp) rs749784223
NM_170707.4(LMNA):c.1028G>A (p.Arg343Gln) rs61177390
NM_170707.4(LMNA):c.109G>A (p.Glu37Lys) rs1354642495
NM_170707.4(LMNA):c.1187A>T (p.Gln396Leu) rs61693978
NM_170707.4(LMNA):c.1195C>T (p.Arg399Cys) rs58672172
NM_170707.4(LMNA):c.1196G>A (p.Arg399His) rs267607563
NM_170707.4(LMNA):c.1202G>A (p.Arg401His) rs141490569
NM_170707.4(LMNA):c.1230G>A (p.Gln410=)
NM_170707.4(LMNA):c.1232G>A (p.Gly411Asp) rs267607647
NM_170707.4(LMNA):c.1247C>A (p.Thr416Asn)
NM_170707.4(LMNA):c.1255C>T (p.Arg419Cys) rs755686359
NM_170707.4(LMNA):c.1262T>C (p.Leu421Pro) rs267607564
NM_170707.4(LMNA):c.1279C>T (p.Arg427Cys) rs373584456
NM_170707.4(LMNA):c.1286G>A (p.Ser429Asn)
NM_170707.4(LMNA):c.1295A>G (p.Gln432Arg)
NM_170707.4(LMNA):c.1312G>A (p.Gly438Arg)
NM_170707.4(LMNA):c.1315C>T (p.Arg439Cys) rs62636506
NM_170707.4(LMNA):c.1318G>A (p.Val440Met) rs121912493
NM_170707.4(LMNA):c.1324G>A (p.Val442Met) rs368542816
NM_170707.4(LMNA):c.1327G>A (p.Glu443Lys) rs1558132212
NM_170707.4(LMNA):c.1338T>G (p.Asp446Glu)
NM_170707.4(LMNA):c.1358G>A (p.Arg453Gln) rs267607598
NM_170707.4(LMNA):c.1364G>A (p.Arg455His)
NM_170707.4(LMNA):c.1380+3A>G
NM_170707.4(LMNA):c.1381-5G>A rs730880133
NM_170707.4(LMNA):c.1381G>T (p.Asp461Tyr) rs267607642
NM_170707.4(LMNA):c.1390A>G (p.Met464Val) rs200262654
NM_170707.4(LMNA):c.141C>A (p.Asp47Glu)
NM_170707.4(LMNA):c.1422_1424dup (p.Asp475_Asp476insGlu) rs267607579
NM_170707.4(LMNA):c.1453C>G (p.Pro485Ala) rs886042993
NM_170707.4(LMNA):c.1487C>T (p.Thr496Met) rs200466188
NM_170707.4(LMNA):c.1488+6T>G rs369642101
NM_170707.4(LMNA):c.1517A>C (p.His506Pro) rs878855233
NM_170707.4(LMNA):c.1531G>A (p.Asp511Asn) rs759408439
NM_170707.4(LMNA):c.1546G>A (p.Ala516Thr)
NM_170707.4(LMNA):c.1579C>T (p.Arg527Cys) rs57318642
NM_170707.4(LMNA):c.1580G>A (p.Arg527His) rs57520892
NM_170707.4(LMNA):c.1580G>T (p.Arg527Leu)
NM_170707.4(LMNA):c.1583C>T (p.Thr528Met) rs57629361
NM_170707.4(LMNA):c.1604G>A (p.Gly535Glu) rs747717293
NM_170707.4(LMNA):c.161C>T (p.Thr54Met) rs879253992
NM_170707.4(LMNA):c.1642A>C (p.Thr548Pro)
NM_170707.4(LMNA):c.1696C>G (p.His566Asp) rs1195284382
NM_170707.4(LMNA):c.1698+13C>A rs80338938
NM_170707.4(LMNA):c.1698+13C>T rs80338938
NM_170707.4(LMNA):c.1699-9_1699-8del rs1572369030
NM_170707.4(LMNA):c.1718C>T (p.Ser573Leu) rs60890628
NM_170707.4(LMNA):c.1729G>A (p.Ala577Thr) rs1439261714
NM_170707.4(LMNA):c.1747_1750dup (p.Arg584fs)
NM_170707.4(LMNA):c.1748C>T (p.Ser583Leu) rs59601651
NM_170707.4(LMNA):c.1750C>T (p.Arg584Cys) rs578193315
NM_170707.4(LMNA):c.1751G>A (p.Arg584His) rs56657623
NM_170707.4(LMNA):c.1765G>A (p.Gly589Arg) rs372201662
NM_170707.4(LMNA):c.1817A>G (p.Gln606Arg)
NM_170707.4(LMNA):c.1835C>T (p.Ser612Phe)
NM_170707.4(LMNA):c.1862C>T (p.Thr621Met) rs765594825
NM_170707.4(LMNA):c.1867A>G (p.Thr623Ala) rs757888891
NM_170707.4(LMNA):c.1871G>A (p.Arg624His) rs13768
NM_170707.4(LMNA):c.1873A>T (p.Ser625Cys) rs398124550
NM_170707.4(LMNA):c.1873_1874delinsCC (p.Ser625Pro) rs1553266553
NM_170707.4(LMNA):c.1879C>T (p.Arg627Cys) rs777841827
NM_170707.4(LMNA):c.1891G>A (p.Gly631Ser) rs951584348
NM_170707.4(LMNA):c.1901G>A (p.Gly634Asp)
NM_170707.4(LMNA):c.1911C>A (p.Phe637Leu) rs117939448
NM_170707.4(LMNA):c.1916A>G (p.Asp639Gly)
NM_170707.4(LMNA):c.1922T>G (p.Leu641Arg)
NM_170707.4(LMNA):c.1943T>G (p.Leu648Arg)
NM_170707.4(LMNA):c.1961G>A (p.Arg654Gln)
NM_170707.4(LMNA):c.1969-11T>G
NM_170707.4(LMNA):c.1969-1G>T rs1060499873
NM_170707.4(LMNA):c.1978A>G (p.Asn660Asp) rs374926367
NM_170707.4(LMNA):c.202G>A (p.Glu68Lys)
NM_170707.4(LMNA):c.206T>C (p.Val69Ala)
NM_170707.4(LMNA):c.20G>A (p.Arg7Gln) rs751916168
NM_170707.4(LMNA):c.215G>A (p.Arg72His)
NM_170707.4(LMNA):c.286G>T (p.Ala96Ser) rs1553262000
NM_170707.4(LMNA):c.293A>G (p.Glu98Gly)
NM_170707.4(LMNA):c.328C>A (p.Arg110Ser) rs1064797121
NM_170707.4(LMNA):c.329G>A (p.Arg110His) rs556237236
NM_170707.4(LMNA):c.373G>A (p.Gly125Ser) rs267607605
NM_170707.4(LMNA):c.383T>C (p.Ile128Thr)
NM_170707.4(LMNA):c.386C>A (p.Ala129Asp) rs768203943
NM_170707.4(LMNA):c.398G>A (p.Arg133Gln) rs60864230
NM_170707.4(LMNA):c.488A>G (p.His163Arg)
NM_170707.4(LMNA):c.489T>G (p.His163Gln) rs1558126350
NM_170707.4(LMNA):c.511A>G (p.Lys171Glu)
NM_170707.4(LMNA):c.521C>A (p.Ala174Glu)
NM_170707.4(LMNA):c.536C>A (p.Ala179Asp)
NM_170707.4(LMNA):c.554A>T (p.Asp185Val)
NM_170707.4(LMNA):c.565C>T (p.Arg189Trp) rs267607626
NM_170707.4(LMNA):c.566G>A (p.Arg189Gln) rs766856162
NM_170707.4(LMNA):c.610C>G (p.Leu204Val) rs1553265177
NM_170707.4(LMNA):c.647G>A (p.Arg216His) rs757041809
NM_170707.4(LMNA):c.658C>T (p.Arg220Cys) rs370134870
NM_170707.4(LMNA):c.659G>A (p.Arg220His)
NM_170707.4(LMNA):c.674G>A (p.Arg225Gln) rs199474724
NM_170707.4(LMNA):c.692A>G (p.Asn231Ser)
NM_170707.4(LMNA):c.704G>A (p.Arg235His) rs759829161
NM_170707.4(LMNA):c.74G>T (p.Arg25Leu) rs61578124
NM_170707.4(LMNA):c.760G>A (p.Asp254Asn) rs1553265346
NM_170707.4(LMNA):c.784_785delinsTT (p.Glu262Leu)
NM_170707.4(LMNA):c.787C>A (p.Leu263Met) rs750246389
NM_170707.4(LMNA):c.848A>G (p.Asn283Ser) rs765241364
NM_170707.4(LMNA):c.853G>T (p.Val285Leu) rs746056534
NM_170707.4(LMNA):c.860C>T (p.Ala287Val) rs397517910
NM_170707.4(LMNA):c.877C>G (p.Gln293Glu)
NM_170707.4(LMNA):c.884C>T (p.Ser295Leu) rs769210828
NM_170707.4(LMNA):c.886C>T (p.Arg296Cys) rs375987939
NM_170707.4(LMNA):c.889A>G (p.Ile297Val) rs886043082
NM_170707.4(LMNA):c.892C>T (p.Arg298Cys) rs59885338
NM_170707.4(LMNA):c.897C>G (p.Ile299Met) rs762718963
NM_170707.4(LMNA):c.8C>A (p.Thr3Asn)
NM_170707.4(LMNA):c.937-7C>G rs267607681
NM_170707.4(LMNA):c.952G>A (p.Ala318Thr) rs267607574
NM_170707.4(LMNA):c.953C>T (p.Ala318Val) rs1212920276
NM_170707.4(LMNA):c.977C>T (p.Ser326Leu)
NM_170707.4(LMNA):c.985C>T (p.Arg329Cys) rs775159300
NM_170707.4(LMNA):c.986G>A (p.Arg329His) rs397517913
NM_170707.4(LMNA):c.991C>T (p.Arg331Trp) rs879253898

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.