ClinVar Miner

List of variants in gene NSUN2 studied for not specified

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Gene type:
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Total variants: 42
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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.1226+4A>T rs202085420 0.00041
NM_017755.6(NSUN2):c.915C>T (p.Arg305=) rs527650370 0.00021
NM_017755.6(NSUN2):c.762C>T (p.Asp254=) rs763930477 0.00016
NM_017755.6(NSUN2):c.1010A>G (p.Glu337Gly) rs758250936 0.00011
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.1046C>T (p.Ser349Phe) rs200175285 0.00008
NM_017755.6(NSUN2):c.2137G>A (p.Glu713Lys) rs200232369 0.00008
NM_017755.6(NSUN2):c.1185G>A (p.Pro395=) rs536258085 0.00007
NM_017755.6(NSUN2):c.891-3T>C rs765461729 0.00006
NM_017755.6(NSUN2):c.1804C>T (p.Arg602Trp) rs371887249 0.00003
NM_017755.6(NSUN2):c.2259C>T (p.Asp753=) rs372574598 0.00003
NM_017755.6(NSUN2):c.2280G>C (p.Pro760=) rs150472251 0.00003
NM_017755.6(NSUN2):c.763G>A (p.Gly255Ser) rs140003855 0.00003
NM_017755.6(NSUN2):c.1223G>A (p.Arg408Gln) rs1056148130 0.00002
NM_017755.6(NSUN2):c.174G>A (p.Val58=) rs745966593 0.00002
NM_017755.6(NSUN2):c.1103C>T (p.Thr368Met) rs200705396 0.00001
NM_017755.6(NSUN2):c.1932G>T (p.Glu644Asp) rs372753280 0.00001
NM_017755.6(NSUN2):c.354G>C (p.Leu118=) rs1479645177 0.00001
NM_017755.6(NSUN2):c.822C>T (p.Asp274=) rs141802308 0.00001
NM_017755.6(NSUN2):c.1450A>G (p.Ile484Val) rs899944658
NM_017755.6(NSUN2):c.1819-12_1819-11del rs1553996635
NM_017755.6(NSUN2):c.1946C>T (p.Ala649Val) rs1351714861
NM_017755.6(NSUN2):c.1998-8A>G rs797045836
NM_017755.6(NSUN2):c.2022C>T (p.Pro674=) rs797045837
NM_017755.6(NSUN2):c.2218G>A (p.Glu740Lys) rs1368308800
NM_017755.6(NSUN2):c.2279C>A (p.Pro760Gln) rs61744358
NM_017755.6(NSUN2):c.360-7_360-5delinsCGC rs2126504490
NM_017755.6(NSUN2):c.97-10C>T rs199959678

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