ClinVar Miner

List of variants in gene NIPBL reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 105
Download table as spreadsheet
HGVS dbSNP
NM_133433.3(NIPBL):c.-80+5delA rs532015680
NM_133433.3(NIPBL):c.5863-12_5863-11dupAT rs10554564
NM_133433.4(NIPBL):c.-243A>C rs544681871
NM_133433.4(NIPBL):c.-307C>T rs377354585
NM_133433.4(NIPBL):c.-312T>A rs540966156
NM_133433.4(NIPBL):c.-429del rs376839773
NM_133433.4(NIPBL):c.1056C>T (p.Ser352=) rs200440893
NM_133433.4(NIPBL):c.1164T>C (p.Asn388=) rs768113851
NM_133433.4(NIPBL):c.1212C>T (p.Pro404=) rs80358349
NM_133433.4(NIPBL):c.126T>C (p.Phe42=) rs727504046
NM_133433.4(NIPBL):c.1302G>C (p.Val434=) rs769279620
NM_133433.4(NIPBL):c.1392T>A (p.Pro464=) rs555179389
NM_133433.4(NIPBL):c.1495+8_1495+10del rs398124464
NM_133433.4(NIPBL):c.1526C>G (p.Ser509Cys) rs80358352
NM_133433.4(NIPBL):c.179A>G (p.Asn60Ser) rs142703446
NM_133433.4(NIPBL):c.1891G>T (p.Val631Leu)
NM_133433.4(NIPBL):c.1965G>T (p.Glu655Asp) rs80358350
NM_133433.4(NIPBL):c.1985A>G (p.Lys662Arg) rs140100861
NM_133433.4(NIPBL):c.198C>G (p.Val66=) rs146033170
NM_133433.4(NIPBL):c.2120G>T (p.Gly707Val)
NM_133433.4(NIPBL):c.2294G>A (p.Arg765Lys) rs185678374
NM_133433.4(NIPBL):c.2349A>G (p.Lys783=)
NM_133433.4(NIPBL):c.2375G>T (p.Arg792Leu)
NM_133433.4(NIPBL):c.2447G>A (p.Arg816His) rs80358359
NM_133433.4(NIPBL):c.2469A>G (p.Lys823=) rs293756
NM_133433.4(NIPBL):c.2471C>T (p.Ser824Leu) rs587783904
NM_133433.4(NIPBL):c.2592T>A (p.Asp864Glu) rs80358365
NM_133433.4(NIPBL):c.2673C>T (p.Asp891=) rs376637245
NM_133433.4(NIPBL):c.2727T>C (p.Gly909=) rs148394805
NM_133433.4(NIPBL):c.2768G>T (p.Gly923Val) rs200991784
NM_133433.4(NIPBL):c.2931A>G (p.Glu977=) rs587783913
NM_133433.4(NIPBL):c.294C>T (p.Ala98=) rs142184978
NM_133433.4(NIPBL):c.3015A>G (p.Leu1005=) rs1669445
NM_133433.4(NIPBL):c.3121+11T>G rs457583
NM_133433.4(NIPBL):c.3126T>C (p.Ser1042=) rs757245118
NM_133433.4(NIPBL):c.3204T>C (p.Arg1068=)
NM_133433.4(NIPBL):c.3347A>G (p.Glu1116Gly) rs552620284
NM_133433.4(NIPBL):c.3423A>G (p.Ser1141=) rs571024836
NM_133433.4(NIPBL):c.3502+17A>C rs144725401
NM_133433.4(NIPBL):c.3541A>C (p.Arg1181=) rs35748854
NM_133433.4(NIPBL):c.3574+20A>C rs530238141
NM_133433.4(NIPBL):c.3575-17A>G rs78827246
NM_133433.4(NIPBL):c.3630G>A (p.Leu1210=)
NM_133433.4(NIPBL):c.3660G>A (p.Ala1220=) rs143252734
NM_133433.4(NIPBL):c.3768+34T>G rs149115930
NM_133433.4(NIPBL):c.3897T>C (p.Leu1299=) rs80358354
NM_133433.4(NIPBL):c.4203A>G (p.Leu1401=) rs1356246775
NM_133433.4(NIPBL):c.4240-14T>G rs298972
NM_133433.4(NIPBL):c.4240-7T>C rs587783943
NM_133433.4(NIPBL):c.4245A>C (p.Ser1415=) rs138440449
NM_133433.4(NIPBL):c.42G>A (p.Ala14=) rs727504045
NM_133433.4(NIPBL):c.4305T>C (p.Ile1435=)
NM_133433.4(NIPBL):c.4320+14A>G rs377381536
NM_133433.4(NIPBL):c.4321-35T>C
NM_133433.4(NIPBL):c.435C>T (p.Thr145=) rs1561082537
NM_133433.4(NIPBL):c.4421+7A>G rs76297333
NM_133433.4(NIPBL):c.4535A>T (p.Asn1512Ile) rs587783949
NM_133433.4(NIPBL):c.4561-10T>C
NM_133433.4(NIPBL):c.4561-9T>A rs79924167
NM_133433.4(NIPBL):c.4731A>G (p.Glu1577=) rs140021654
NM_133433.4(NIPBL):c.4773G>C (p.Leu1591=)
NM_133433.4(NIPBL):c.4776+12G>A rs199632698
NM_133433.4(NIPBL):c.4777-12T>C rs80358381
NM_133433.4(NIPBL):c.4959A>G (p.Lys1653=) rs145952190
NM_133433.4(NIPBL):c.5101T>C (p.Ser1701Pro) rs139819353
NM_133433.4(NIPBL):c.5226-14A>G rs587783964
NM_133433.4(NIPBL):c.5226-4G>A rs370826969
NM_133433.4(NIPBL):c.534C>T (p.Tyr178=) rs148542094
NM_133433.4(NIPBL):c.535G>A (p.Ala179Thr) rs142923613
NM_133433.4(NIPBL):c.5472G>A (p.Ser1824=) rs369177620
NM_133433.4(NIPBL):c.5690A>G (p.Asn1897Ser) rs190086412
NM_133433.4(NIPBL):c.5709+4G>A rs370325589
NM_133433.4(NIPBL):c.5710-13C>T rs562131143
NM_133433.4(NIPBL):c.5762A>G (p.Asn1921Ser) rs587783983
NM_133433.4(NIPBL):c.5863-10_5863-3dup rs1554029659
NM_133433.4(NIPBL):c.5863-16A>G rs578098911
NM_133433.4(NIPBL):c.5979C>T (p.Asp1993=) rs761030463
NM_133433.4(NIPBL):c.6069T>C (p.His2023=) rs1561196903
NM_133433.4(NIPBL):c.6109-3T>C rs145778995
NM_133433.4(NIPBL):c.6145A>G (p.Lys2049Glu) rs587783996
NM_133433.4(NIPBL):c.615G>A (p.Ser205=) rs150678035
NM_133433.4(NIPBL):c.6250-6T>C rs587784001
NM_133433.4(NIPBL):c.6322G>A (p.Ala2108Thr) rs587784006
NM_133433.4(NIPBL):c.6400C>T (p.Leu2134=) rs372730081
NM_133433.4(NIPBL):c.6438C>T (p.Thr2146=) rs376448686
NM_133433.4(NIPBL):c.65-5A>C
NM_133433.4(NIPBL):c.6589+9A>T rs370709104
NM_133433.4(NIPBL):c.6613A>G (p.Ser2205Gly) rs587784018
NM_133433.4(NIPBL):c.6624C>T (p.Phe2208=)
NM_133433.4(NIPBL):c.6645A>G (p.Leu2215=) rs149186951
NM_133433.4(NIPBL):c.6764-4G>C rs757590127
NM_133433.4(NIPBL):c.6769A>G (p.Lys2257Glu) rs947067048
NM_133433.4(NIPBL):c.7245C>T (p.Asn2415=) rs1561216202
NM_133433.4(NIPBL):c.7463A>G (p.Asn2488Ser) rs794727675
NM_133433.4(NIPBL):c.7590A>G (p.Ser2530=) rs1286310849
NM_133433.4(NIPBL):c.7641C>T (p.Leu2547=) rs587784046
NM_133433.4(NIPBL):c.7727A>G (p.Tyr2576Cys) rs80358351
NM_133433.4(NIPBL):c.781T>G (p.Ser261Ala) rs16903425
NM_133433.4(NIPBL):c.7830G>C (p.Val2610=) rs115668015
NM_133433.4(NIPBL):c.804A>G (p.Ala268=)
NM_133433.4(NIPBL):c.862C>A (p.Pro288Thr) rs546188623
NM_133433.4(NIPBL):c.87A>G (p.Pro29=) rs587784061
NM_133433.4(NIPBL):c.891A>C (p.Leu297=) rs373684382
NM_133433.4(NIPBL):c.915A>G (p.Ser305=)
NM_133433.4(NIPBL):c.961A>C (p.Arg321=)

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.