ClinVar Miner

List of variants in gene NSD1 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 113
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_022455.5(NSD1):c.2032A>G (p.Met678Val) rs773904155 0.00003
NM_022455.5(NSD1):c.2297C>T (p.Ser766Leu) rs773591859 0.00002
NM_022455.5(NSD1):c.1646A>C (p.Asn549Thr) rs756449994 0.00001
NM_022455.5(NSD1):c.3766T>A (p.Leu1256Met) rs1276998178 0.00001
NM_022455.5(NSD1):c.3836A>G (p.Lys1279Arg) rs1765400330 0.00001
NM_022455.5(NSD1):c.383A>G (p.Gln128Arg) rs764617265 0.00001
NM_022455.5(NSD1):c.4150C>T (p.Arg1384Trp) rs1765619618 0.00001
NM_022455.5(NSD1):c.4724A>T (p.Glu1575Val) rs1237319595 0.00001
NM_022455.5(NSD1):c.653G>T (p.Arg218Ile) rs1240149522 0.00001
NM_022455.5(NSD1):c.7487G>T (p.Gly2496Val) rs556993869 0.00001
NM_022455.5(NSD1):c.7739C>T (p.Ala2580Val) rs755285941 0.00001
NM_022455.5(NSD1):c.105T>G (p.Gly35=) rs2149755343
NM_022455.5(NSD1):c.1096G>A (p.Val366Met) rs1172667661
NM_022455.5(NSD1):c.1129T>C (p.Trp377Arg) rs1762711811
NM_022455.5(NSD1):c.1204G>C (p.Gly402Arg) rs1762715103
NM_022455.5(NSD1):c.1325G>A (p.Cys442Tyr) rs1763180633
NM_022455.5(NSD1):c.1372G>A (p.Glu458Lys)
NM_022455.5(NSD1):c.1372G>C (p.Glu458Gln) rs2149842728
NM_022455.5(NSD1):c.145C>T (p.Gln49Ter) rs1336273625
NM_022455.5(NSD1):c.1554T>G (p.Phe518Leu)
NM_022455.5(NSD1):c.1562A>G (p.His521Arg)
NM_022455.5(NSD1):c.1621G>A (p.Asp541Asn)
NM_022455.5(NSD1):c.1676C>T (p.Thr559Ile)
NM_022455.5(NSD1):c.173A>G (p.Gln58Arg)
NM_022455.5(NSD1):c.1769T>C (p.Leu590Ser) rs1763219171
NM_022455.5(NSD1):c.1775G>A (p.Gly592Asp)
NM_022455.5(NSD1):c.1837C>G (p.Leu613Val)
NM_022455.5(NSD1):c.1964G>A (p.Ser655Asn)
NM_022455.5(NSD1):c.1980C>A (p.Asn660Lys) rs140072393
NM_022455.5(NSD1):c.2408C>G (p.Pro803Arg) rs1763279245
NM_022455.5(NSD1):c.2452G>A (p.Asp818Asn)
NM_022455.5(NSD1):c.2503G>A (p.Gly835Ser) rs1197555000
NM_022455.5(NSD1):c.2528A>T (p.His843Leu)
NM_022455.5(NSD1):c.2668T>G (p.Phe890Val) rs1763299227
NM_022455.5(NSD1):c.2670C>G (p.Phe890Leu)
NM_022455.5(NSD1):c.2831G>A (p.Cys944Tyr)
NM_022455.5(NSD1):c.2947G>A (p.Gly983Ser) rs373280032
NM_022455.5(NSD1):c.3055C>G (p.Arg1019Gly)
NM_022455.5(NSD1):c.3193G>T (p.Asp1065Tyr)
NM_022455.5(NSD1):c.3224G>A (p.Gly1075Glu) rs1562212091
NM_022455.5(NSD1):c.3277A>C (p.Ile1093Leu)
NM_022455.5(NSD1):c.3323T>C (p.Val1108Ala) rs779656661
NM_022455.5(NSD1):c.334G>T (p.Val112Phe) rs1756231832
NM_022455.5(NSD1):c.3358G>C (p.Gly1120Arg) rs1763362171
NM_022455.5(NSD1):c.3422T>G (p.Met1141Arg)
NM_022455.5(NSD1):c.3460G>A (p.Val1154Met) rs1001657669
NM_022455.5(NSD1):c.3664A>G (p.Asn1222Asp)
NM_022455.5(NSD1):c.3671C>G (p.Ala1224Gly)
NM_022455.5(NSD1):c.3706G>A (p.Val1236Ile)
NM_022455.5(NSD1):c.3758T>C (p.Ile1253Thr)
NM_022455.5(NSD1):c.3796G>A (p.Ala1266Thr) rs2149849787
NM_022455.5(NSD1):c.3870G>T (p.Gln1290His)
NM_022455.5(NSD1):c.3874T>A (p.Phe1292Ile)
NM_022455.5(NSD1):c.3894_3896del (p.Lys1300del) rs2149884022
NM_022455.5(NSD1):c.398A>G (p.Asn133Ser)
NM_022455.5(NSD1):c.3997A>G (p.Asn1333Asp)
NM_022455.5(NSD1):c.4020A>G (p.Glu1340=) rs2149887388
NM_022455.5(NSD1):c.438C>G (p.Ile146Met) rs1240259079
NM_022455.5(NSD1):c.4403C>T (p.Pro1468Leu)
NM_022455.5(NSD1):c.4484T>G (p.Ile1495Ser) rs1554197510
NM_022455.5(NSD1):c.4501G>A (p.Glu1501Lys)
NM_022455.5(NSD1):c.4531C>A (p.Pro1511Thr)
NM_022455.5(NSD1):c.4691G>A (p.Gly1564Glu)
NM_022455.5(NSD1):c.4701C>A (p.His1567Gln) rs2149904507
NM_022455.5(NSD1):c.4748G>T (p.Cys1583Phe) rs2149904611
NM_022455.5(NSD1):c.4765+4A>G rs1554198443
NM_022455.5(NSD1):c.4783G>C (p.Val1595Leu)
NM_022455.5(NSD1):c.4826C>T (p.Pro1609Leu) rs2149912363
NM_022455.5(NSD1):c.4913A>G (p.His1638Arg)
NM_022455.5(NSD1):c.4987C>T (p.Arg1663Cys) rs587784134
NM_022455.5(NSD1):c.5150G>A (p.Gly1717Asp) rs2149930984
NM_022455.5(NSD1):c.5565A>T (p.Arg1855Ser) rs2127241925
NM_022455.5(NSD1):c.5651T>A (p.Ile1884Asn)
NM_022455.5(NSD1):c.5714G>C (p.Cys1905Ser) rs1554204110
NM_022455.5(NSD1):c.5741G>A (p.Arg1914His) rs587784155
NM_022455.5(NSD1):c.5789G>A (p.Arg1930His) rs1391504793
NM_022455.5(NSD1):c.5816G>T (p.Arg1939Leu)
NM_022455.5(NSD1):c.5827G>A (p.Glu1943Lys) rs2127257497
NM_022455.5(NSD1):c.5836A>G (p.Ile1946Val)
NM_022455.5(NSD1):c.5842C>T (p.Arg1948Cys) rs886041941
NM_022455.5(NSD1):c.5878A>G (p.Thr1960Ala)
NM_022455.5(NSD1):c.5890A>G (p.Lys1964Glu) rs2127257672
NM_022455.5(NSD1):c.5960A>G (p.Tyr1987Cys)
NM_022455.5(NSD1):c.6010-11T>A rs1554204909
NM_022455.5(NSD1):c.6200A>T (p.Lys2067Met) rs1759549616
NM_022455.5(NSD1):c.622G>A (p.Gly208Arg) rs1581091469
NM_022455.5(NSD1):c.6314G>A (p.Gly2105Glu)
NM_022455.5(NSD1):c.6430G>A (p.Ala2144Thr) rs761103348
NM_022455.5(NSD1):c.6443A>G (p.Asn2148Ser) rs2127276605
NM_022455.5(NSD1):c.6479C>T (p.Pro2160Leu)
NM_022455.5(NSD1):c.649_650del (p.Glu216_Ser217insTer) rs1562098870
NM_022455.5(NSD1):c.662C>T (p.Ala221Val) rs1057524420
NM_022455.5(NSD1):c.6818G>C (p.Cys2273Ser)
NM_022455.5(NSD1):c.6824G>A (p.Arg2275Lys)
NM_022455.5(NSD1):c.6967G>T (p.Ala2323Ser)
NM_022455.5(NSD1):c.7046C>G (p.Pro2349Arg)
NM_022455.5(NSD1):c.7159C>G (p.Pro2387Ala) rs1416255762
NM_022455.5(NSD1):c.7219A>G (p.Thr2407Ala) rs1057524329
NM_022455.5(NSD1):c.7259C>T (p.Pro2420Leu) rs1271164466
NM_022455.5(NSD1):c.7419T>G (p.His2473Gln)
NM_022455.5(NSD1):c.7433A>G (p.Gln2478Arg)
NM_022455.5(NSD1):c.7510G>A (p.Val2504Ile) rs1005975383
NM_022455.5(NSD1):c.7525G>T (p.Val2509Leu)
NM_022455.5(NSD1):c.7573G>C (p.Asp2525His)
NM_022455.5(NSD1):c.7604A>G (p.Gln2535Arg) rs2127283711
NM_022455.5(NSD1):c.7949_7950delinsTT (p.Trp2650Phe) rs2127285025
NM_022455.5(NSD1):c.8032C>G (p.Leu2678Val) rs2127285369
NM_022455.5(NSD1):c.805G>A (p.Glu269Lys) rs751787444
NM_022455.5(NSD1):c.8075_8076insTT (p.Glu2692fs) rs2127285539
NM_022455.5(NSD1):c.817T>C (p.Ser273Pro)
NM_022455.5(NSD1):c.872A>G (p.Asn291Ser)
NM_022455.5(NSD1):c.887C>A (p.Pro296His)
NM_022455.5(NSD1):c.927+3A>T

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.