ClinVar Miner

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

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Gene type:
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Total variants: 60
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HGVS dbSNP
NM_022455.4(NSD1):c.1047A>G (p.Thr349=) rs1581254386
NM_022455.4(NSD1):c.1064-5C>A rs961502921
NM_022455.4(NSD1):c.1173A>G (p.Gln391=) rs146581653
NM_022455.4(NSD1):c.1499G>C (p.Arg500Thr) rs867877508
NM_022455.4(NSD1):c.1500A>G (p.Arg500=) rs1469000222
NM_022455.4(NSD1):c.1716C>T (p.Ser572=) rs375093905
NM_022455.4(NSD1):c.1813G>C (p.Glu605Gln) rs971996804
NM_022455.4(NSD1):c.1830A>G (p.Gln610=) rs759706066
NM_022455.4(NSD1):c.2031T>G (p.Ser677=) rs143705256
NM_022455.4(NSD1):c.2331A>C (p.Leu777=) rs772447375
NM_022455.4(NSD1):c.2340G>A (p.Ser780=) rs766703389
NM_022455.4(NSD1):c.2345G>A (p.Ser782Asn) rs769773081
NM_022455.4(NSD1):c.2475C>T (p.Ala825=) rs781498491
NM_022455.4(NSD1):c.2581T>C (p.Leu861=) rs1393651252
NM_022455.4(NSD1):c.2652A>G (p.Pro884=) rs1060504243
NM_022455.4(NSD1):c.2696T>C (p.Ile899Thr) rs142703625
NM_022455.4(NSD1):c.2748T>G (p.Asp916Glu) rs1268847680
NM_022455.4(NSD1):c.2766G>A (p.Thr922=) rs369705297
NM_022455.4(NSD1):c.2968G>A (p.Glu990Lys) rs138673583
NM_022455.4(NSD1):c.2991C>T (p.Gly997=) rs751017119
NM_022455.4(NSD1):c.3088T>C (p.Leu1030=) rs61756006
NM_022455.4(NSD1):c.3089T>C (p.Leu1030Ser) rs200856103
NM_022455.4(NSD1):c.3090G>T (p.Leu1030Phe) rs201860097
NM_022455.4(NSD1):c.3307G>A (p.Asp1103Asn) rs746210838
NM_022455.4(NSD1):c.3921+9C>T rs192246663
NM_022455.4(NSD1):c.39G>C (p.Leu13=) rs1581089158
NM_022455.4(NSD1):c.4188G>T (p.Thr1396=) rs148112060
NM_022455.4(NSD1):c.4379-5C>T rs763154004
NM_022455.4(NSD1):c.4497+141A>G rs71601347
NM_022455.4(NSD1):c.4509G>A (p.Met1503Ile) rs199574095
NM_022455.4(NSD1):c.4521G>A (p.Thr1507=) rs778642917
NM_022455.4(NSD1):c.454C>T (p.His152Tyr) rs765845162
NM_022455.4(NSD1):c.4564G>T (p.Asp1522Tyr) rs201483724
NM_022455.4(NSD1):c.4766-9G>T rs747358179
NM_022455.4(NSD1):c.4892A>G (p.Lys1631Arg) rs201857437
NM_022455.4(NSD1):c.5103T>C (p.Asn1701=) rs756895271
NM_022455.4(NSD1):c.530A>G (p.Asp177Gly) rs538618950
NM_022455.4(NSD1):c.5382C>T (p.Phe1794=) rs878855076
NM_022455.4(NSD1):c.5457C>T (p.Asp1819=) rs1211226803
NM_022455.4(NSD1):c.5610T>C (p.Tyr1870=) rs1581507735
NM_022455.4(NSD1):c.5892+7A>T rs769311050
NM_022455.4(NSD1):c.6123C>G (p.Gly2041=) rs1320561007
NM_022455.4(NSD1):c.6152-5T>C rs755758018
NM_022455.4(NSD1):c.622G>A (p.Gly208Arg) rs1581091469
NM_022455.4(NSD1):c.6259-4G>T rs764710462
NM_022455.4(NSD1):c.6444T>C (p.Asn2148=) rs146601031
NM_022455.4(NSD1):c.6463+250C>A rs537540896
NM_022455.4(NSD1):c.6464-5T>C rs545039997
NM_022455.4(NSD1):c.6464-8G>T rs577262396
NM_022455.4(NSD1):c.6468A>G (p.Lys2156=) rs752628095
NM_022455.4(NSD1):c.6513A>C (p.Ala2171=) rs1581562928
NM_022455.4(NSD1):c.7025C>T (p.Ser2342Leu) rs201609442
NM_022455.4(NSD1):c.7160C>T (p.Pro2387Leu) rs766700264
NM_022455.4(NSD1):c.72C>T (p.Ala24=) rs147146776
NM_022455.4(NSD1):c.736G>T (p.Gly246Cys) rs1156510513
NM_022455.4(NSD1):c.7752C>T (p.Val2584=) rs1175003950
NM_022455.4(NSD1):c.8025A>G (p.Gln2675=) rs199895437
NM_022455.4(NSD1):c.804A>G (p.Glu268=) rs766770297
NM_022455.4(NSD1):c.936T>G (p.Pro312=) rs1581254248
NM_172349.2(NSD1):c.31-130G>C rs28932175

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