ClinVar Miner

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

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Gene type:
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Total variants: 73
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HGVS dbSNP
NM_022455.4(NSD1):c.-8G>A rs199639292
NM_022455.4(NSD1):c.1064-10C>T rs1057523596
NM_022455.4(NSD1):c.1236+17G>A rs886038671
NM_022455.4(NSD1):c.1237-37del rs886038672
NM_022455.4(NSD1):c.1495G>A (p.Ala499Thr) rs587784075
NM_022455.4(NSD1):c.1558G>A (p.Ala520Thr) rs559617787
NM_022455.4(NSD1):c.1574G>A (p.Arg525Gln) rs138405802
NM_022455.4(NSD1):c.1596C>T (p.Asn532=) rs1554188977
NM_022455.4(NSD1):c.1690G>T (p.Ala564Ser) rs116520623
NM_022455.4(NSD1):c.1980C>T (p.Asn660=) rs140072393
NM_022455.4(NSD1):c.198A>G (p.Pro66=) rs1057523994
NM_022455.4(NSD1):c.2169C>T (p.Thr723=) rs11948062
NM_022455.4(NSD1):c.2295C>T (p.Asn765=) rs146767413
NM_022455.4(NSD1):c.2450C>T (p.Ser817Phe) rs115722008
NM_022455.4(NSD1):c.2655A>G (p.Ser885=) rs1437774200
NM_022455.4(NSD1):c.2696T>C (p.Ile899Thr) rs142703625
NM_022455.4(NSD1):c.2731C>T (p.Leu911=) rs886038673
NM_022455.4(NSD1):c.2776C>A (p.Arg926=) rs886038674
NM_022455.4(NSD1):c.2944G>C (p.Gly982Arg) rs587784091
NM_022455.4(NSD1):c.3000C>T (p.Ser1000=) rs150854966
NM_022455.4(NSD1):c.3154C>T (p.Arg1052Cys) rs748956033
NM_022455.4(NSD1):c.3389A>G (p.Glu1130Gly) rs113856002
NM_022455.4(NSD1):c.3393C>T (p.Asn1131=) rs150296373
NM_022455.4(NSD1):c.339C>T (p.Cys113=) rs77093936
NM_022455.4(NSD1):c.34T>C (p.Cys12Arg) rs143406017
NM_022455.4(NSD1):c.3512G>A (p.Arg1171His) rs111638717
NM_022455.4(NSD1):c.3564G>C (p.Arg1188Ser) rs199814669
NM_022455.4(NSD1):c.3588G>T (p.Val1196=) rs549662786
NM_022455.4(NSD1):c.3722G>C (p.Ser1241Thr) rs138641637
NM_022455.4(NSD1):c.3796+22A>T rs111663030
NM_022455.4(NSD1):c.3803G>A (p.Arg1268Gln) rs368706736
NM_022455.4(NSD1):c.4192+16G>T rs886038675
NM_022455.4(NSD1):c.4303-4A>G rs775759198
NM_022455.4(NSD1):c.4378+26C>T rs139601377
NM_022455.4(NSD1):c.4473G>A (p.Ser1491=) rs150920473
NM_022455.4(NSD1):c.4564G>A (p.Asp1522Asn) rs201483724
NM_022455.4(NSD1):c.4605C>T (p.Arg1535=) rs140229717
NM_022455.4(NSD1):c.4642-7T>C rs183928380
NM_022455.4(NSD1):c.4765+10A>T rs1554198444
NM_022455.4(NSD1):c.480C>T (p.Asp160=) rs79427433
NM_022455.4(NSD1):c.4858G>A (p.Val1620Ile) rs774169673
NM_022455.4(NSD1):c.4892A>G (p.Lys1631Arg) rs201857437
NM_022455.4(NSD1):c.4966+43G>A rs184344717
NM_022455.4(NSD1):c.507C>T (p.Asp169=) rs201012228
NM_022455.4(NSD1):c.5106T>C (p.His1702=) rs778450121
NM_022455.4(NSD1):c.5147-49A>C rs74436451
NM_022455.4(NSD1):c.5303+37C>A rs115164783
NM_022455.4(NSD1):c.5463C>T (p.Ser1821=) rs1554202211
NM_022455.4(NSD1):c.5520A>G (p.Glu1840=) rs140815139
NM_022455.4(NSD1):c.5623-22G>A rs79098301
NM_022455.4(NSD1):c.5630G>A (p.Arg1877His) rs1554204064
NM_022455.4(NSD1):c.5712C>T (p.Pro1904=) rs756321444
NM_022455.4(NSD1):c.5781C>G (p.Ala1927=) rs61749654
NM_022455.4(NSD1):c.6429C>T (p.His2143=) rs121908068
NM_022455.4(NSD1):c.6444T>C (p.Asn2148=) rs146601031
NM_022455.4(NSD1):c.6464-20A>G rs371359117
NM_022455.4(NSD1):c.6480G>A (p.Pro2160=) rs587784203
NM_022455.4(NSD1):c.6788C>T (p.Ser2263Leu) rs373571733
NM_022455.4(NSD1):c.6829T>C (p.Leu2277=) rs28580074
NM_022455.4(NSD1):c.684A>G (p.Pro228=) rs1057522319
NM_022455.4(NSD1):c.6991G>A (p.Asp2331Asn) rs772981865
NM_022455.4(NSD1):c.7115C>A (p.Pro2372His) rs1057522686
NM_022455.4(NSD1):c.7161G>A (p.Pro2387=) rs369778799
NM_022455.4(NSD1):c.7275A>G (p.Leu2425=) rs139879749
NM_022455.4(NSD1):c.7421A>C (p.Gln2474Pro) rs202220730
NM_022455.4(NSD1):c.7500G>C (p.Met2500Ile) rs770120153
NM_022455.4(NSD1):c.7560A>G (p.Ala2520=) rs587784218
NM_022455.4(NSD1):c.760C>T (p.Leu254Phe) rs149334244
NM_022455.4(NSD1):c.767C>T (p.Ala256Val) rs558302421
NM_022455.4(NSD1):c.7850T>C (p.Leu2617Ser) rs77618751
NM_022455.4(NSD1):c.7955C>T (p.Ala2652Val) rs886038676
NM_022455.4(NSD1):c.8022G>A (p.Glu2674=) rs149632999
NM_022455.4(NSD1):c.8050G>A (p.Ala2684Thr) rs188326949

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