ClinVar Miner

List of variants in gene RANBP2 reported as benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
Download table as spreadsheet
HGVS dbSNP
NM_006267.5(RANBP2):c.-45C>T rs79379002
NM_006267.5(RANBP2):c.1064-13A>T rs192629843
NM_006267.5(RANBP2):c.1456-7A>G rs144029181
NM_006267.5(RANBP2):c.2056-19A>G rs199880095
NM_006267.5(RANBP2):c.2330A>G (p.His777Arg) rs61748146
NM_006267.5(RANBP2):c.2339C>T (p.Pro780Leu) rs61758802
NM_006267.5(RANBP2):c.2550A>G (p.Ser850=) rs826549
NM_006267.5(RANBP2):c.2559T>A (p.Asp853Glu) rs148999619
NM_006267.5(RANBP2):c.2562A>G (p.Gly854=) rs13426055
NM_006267.5(RANBP2):c.2955G>A (p.Pro985=) rs61748147
NM_006267.5(RANBP2):c.2982A>T (p.Ala994=) rs61748148
NM_006267.5(RANBP2):c.3411A>C (p.Pro1137=) rs76461420
NM_006267.5(RANBP2):c.3597G>A (p.Ala1199=) rs17036806
NM_006267.5(RANBP2):c.405+17T>G rs826526
NM_006267.5(RANBP2):c.4443A>G (p.Gly1481=) rs61748149
NM_006267.5(RANBP2):c.5941T>A (p.Ser1981Thr) rs61748150
NM_006267.5(RANBP2):c.637-18G>A rs826577
NM_006267.5(RANBP2):c.6609G>A (p.Ala2203=) rs60199637
NM_006267.5(RANBP2):c.72+11C>G rs113447280
NM_006267.5(RANBP2):c.728T>C (p.Met243Thr) rs139151870
NM_006267.5(RANBP2):c.7754T>C (p.Ile2585Thr) rs145886643
NM_006267.5(RANBP2):c.7849+4A>G rs2949961
NM_006267.5(RANBP2):c.816G>C (p.Leu272Phe) rs76352345
NM_006267.5(RANBP2):c.8407A>G (p.Ile2803Val) rs61758804
NM_006267.5(RANBP2):c.8600-14G>T rs57063709
NM_006267.5(RANBP2):c.9585C>T (p.Gly3195=) rs10185197

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.