ClinVar Miner

List of variants in gene NSD1 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_022455.4(NSD1):c.1064-10C>T rs1057523596
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.198A>G (p.Pro66=) rs1057523994
NM_022455.4(NSD1):c.2295C>T (p.Asn765=) rs146767413
NM_022455.4(NSD1):c.2345G>A (p.Ser782Asn)
NM_022455.4(NSD1):c.2655A>G (p.Ser885=) rs1437774200
NM_022455.4(NSD1):c.3000C>T (p.Ser1000=) rs150854966
NM_022455.4(NSD1):c.3393C>T (p.Asn1131=) rs150296373
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.4303-4A>G rs775759198
NM_022455.4(NSD1):c.4473G>A (p.Ser1491=) rs150920473
NM_022455.4(NSD1):c.4497+141A>G
NM_022455.4(NSD1):c.4564G>A (p.Asp1522Asn) rs201483724
NM_022455.4(NSD1):c.4765+10A>T rs1554198444
NM_022455.4(NSD1):c.4892A>G (p.Lys1631Arg) rs201857437
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.5463C>T (p.Ser1821=) rs1554202211
NM_022455.4(NSD1):c.5520A>G (p.Glu1840=) rs140815139
NM_022455.4(NSD1):c.6429C>T (p.His2143=) rs121908068
NM_022455.4(NSD1):c.6463+250C>A
NM_022455.4(NSD1):c.6464-20A>G rs371359117
NM_022455.4(NSD1):c.6788C>T (p.Ser2263Leu) rs373571733
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.7500G>C (p.Met2500Ile) rs770120153
NM_022455.4(NSD1):c.760C>T (p.Leu254Phe) rs149334244
NM_022455.4(NSD1):c.7850T>C (p.Leu2617Ser) rs77618751
NM_022455.4(NSD1):c.8050G>A (p.Ala2684Thr) rs188326949

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