ClinVar Miner

List of variants in gene NSUN2 reported as likely benign by Genetic Services Laboratory, University of Chicago

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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_017755.6(NSUN2):c.97-6C>T rs10076470 0.34106
NM_017755.6(NSUN2):c.51G>A (p.Glu17=) rs10062086 0.33934
NM_017755.6(NSUN2):c.1749G>A (p.Thr583=) rs13181449 0.16076
NM_017755.6(NSUN2):c.2193C>T (p.Asp731=) rs3822434 0.14485
NM_017755.6(NSUN2):c.622+7A>T rs16877704 0.03788
NM_017755.6(NSUN2):c.21T>C (p.Gly7=) rs184594943 0.01714
NM_017755.6(NSUN2):c.2143G>A (p.Val715Ile) rs112951498 0.00574
NM_017755.6(NSUN2):c.2300G>A (p.Arg767Gln) rs140673211 0.00371
NM_017755.6(NSUN2):c.537+8A>G rs149276590 0.00190
NM_017755.6(NSUN2):c.222C>T (p.Leu74=) rs138716662 0.00159
NM_017755.6(NSUN2):c.2272T>C (p.Cys758Arg) rs149244771 0.00051
NM_017755.6(NSUN2):c.258C>T (p.His86=) rs141912087 0.00044
NM_017755.6(NSUN2):c.762C>T (p.Asp254=) rs763930477 0.00016
NM_017755.6(NSUN2):c.2271C>T (p.Gly757=) rs375443052 0.00011
NM_017755.6(NSUN2):c.561T>C (p.Pro187=) rs186098993 0.00011
NM_017755.6(NSUN2):c.1458T>C (p.His486=) rs200925761 0.00010
NM_017755.6(NSUN2):c.891-3T>C rs765461729 0.00006
NM_017755.6(NSUN2):c.2280G>C (p.Pro760=) rs150472251 0.00003
NM_017755.6(NSUN2):c.354G>C (p.Leu118=) rs1479645177 0.00001
NM_017755.6(NSUN2):c.2279C>A (p.Pro760Gln) rs61744358

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