ClinVar Miner

List of variants in gene NSD1 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_022455.5(NSD1):c.6829T>C (p.Leu2277=) rs28580074 0.84910
NM_022455.5(NSD1):c.5623-22G>A rs79098301 0.04787
NM_022455.5(NSD1):c.2169C>T (p.Thr723=) rs11948062 0.00453
NM_022455.5(NSD1):c.1690G>T (p.Ala564Ser) rs116520623 0.00445
NM_022455.5(NSD1):c.5147-49A>C rs74436451 0.00398
NM_022455.5(NSD1):c.2295C>T (p.Asn765=) rs146767413 0.00196
NM_022455.5(NSD1):c.4378+26C>T rs139601377 0.00189
NM_022455.5(NSD1):c.760C>T (p.Leu254Phe) rs149334244 0.00145
NM_022455.5(NSD1):c.339C>T (p.Cys113=) rs77093936 0.00108
NM_022455.5(NSD1):c.2450C>T (p.Ser817Phe) rs115722008 0.00086
NM_022455.5(NSD1):c.3796+22A>T rs111663030 0.00071
NM_022455.5(NSD1):c.1980C>T (p.Asn660=) rs140072393 0.00069
NM_022455.5(NSD1):c.3389A>G (p.Glu1130Gly) rs113856002 0.00058
NM_022455.5(NSD1):c.3564G>C (p.Arg1188Ser) rs199814669 0.00042
NM_022455.5(NSD1):c.4966+43G>A rs184344717 0.00036
NM_022455.5(NSD1):c.3722G>C (p.Ser1241Thr) rs138641637 0.00035
NM_022455.5(NSD1):c.2696T>C (p.Ile899Thr) rs142703625 0.00028
NM_022455.5(NSD1):c.6444T>C (p.Asn2148=) rs146601031 0.00019
NM_022455.5(NSD1):c.7421A>C (p.Gln2474Pro) rs202220730 0.00016
NM_022455.5(NSD1):c.7576C>T (p.Pro2526Ser) rs373932824 0.00016
NM_022455.5(NSD1):c.4605C>T (p.Arg1535=) rs140229717 0.00010
NM_022455.5(NSD1):c.8022G>A (p.Glu2674=) rs149632999 0.00010
NM_022455.5(NSD1):c.1477C>G (p.Pro493Ala) rs375051877 0.00009
NM_022455.5(NSD1):c.7275A>G (p.Leu2425=) rs139879749 0.00009
NM_022455.5(NSD1):c.4642-7T>C rs183928380 0.00006
NM_022455.5(NSD1):c.684A>G (p.Pro228=) rs1057522319 0.00006
NM_022455.5(NSD1):c.3803G>A (p.Arg1268Gln) rs368706736 0.00005
NM_022455.5(NSD1):c.5712C>T (p.Pro1904=) rs756321444 0.00005
NM_022455.5(NSD1):c.3154C>T (p.Arg1052Cys) rs748956033 0.00003
NM_022455.5(NSD1):c.4858G>A (p.Val1620Ile) rs774169673 0.00003
NM_022455.5(NSD1):c.5106T>C (p.His1702=) rs778450121 0.00003
NM_022455.5(NSD1):c.6001C>T (p.Leu2001=) rs587784172 0.00003
NM_022455.5(NSD1):c.7161G>A (p.Pro2387=) rs369778799 0.00003
NM_022455.5(NSD1):c.7500G>C (p.Met2500Ile) rs770120153 0.00003
NM_022455.5(NSD1):c.767C>T (p.Ala256Val) rs558302421 0.00003
NM_022455.5(NSD1):c.1495G>A (p.Ala499Thr) rs587784075 0.00002
NM_022455.5(NSD1):c.198A>G (p.Pro66=) rs1057523994 0.00002
NM_022455.5(NSD1):c.2944G>C (p.Gly982Arg) rs587784091 0.00001
NM_022455.5(NSD1):c.34T>C (p.Cys12Arg) rs143406017 0.00001
NM_022455.5(NSD1):c.6480G>A (p.Pro2160=) rs587784203 0.00001
NM_022455.5(NSD1):c.8050G>A (p.Ala2684Thr) rs188326949 0.00001
NM_022455.5(NSD1):c.1064-10C>T rs1057523596
NM_022455.5(NSD1):c.1236+17G>A rs886038671
NM_022455.5(NSD1):c.1237-37del rs886038672
NM_022455.5(NSD1):c.1596C>T (p.Asn532=) rs1554188977
NM_022455.5(NSD1):c.2655A>G (p.Ser885=) rs1437774200
NM_022455.5(NSD1):c.2731C>T (p.Leu911=) rs886038673
NM_022455.5(NSD1):c.2776C>A (p.Arg926=) rs886038674
NM_022455.5(NSD1):c.4192+16G>T rs886038675
NM_022455.5(NSD1):c.4765+10A>T rs1554198444
NM_022455.5(NSD1):c.507C>T (p.Asp169=) rs201012228
NM_022455.5(NSD1):c.5303+37C>A rs115164783
NM_022455.5(NSD1):c.5630G>A (p.Arg1877His) rs1554204064
NM_022455.5(NSD1):c.5781C>G (p.Ala1927=) rs61749654
NM_022455.5(NSD1):c.7115C>A (p.Pro2372His) rs1057522686
NM_022455.5(NSD1):c.7560A>G (p.Ala2520=) rs587784218
NM_022455.5(NSD1):c.7955C>T (p.Ala2652Val) rs886038676

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