ClinVar Miner

List of variants in gene NSD1 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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Gene type:
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Total variants: 35
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HGVS dbSNP
NM_022455.4(NSD1):c.-8G>A rs199639292
NM_022455.4(NSD1):c.108A>G (p.Gln36=) rs549091873
NM_022455.4(NSD1):c.1149C>T (p.Ile383=) rs34921128
NM_022455.4(NSD1):c.1224A>G (p.Gly408=) rs587784069
NM_022455.4(NSD1):c.1237-10T>C rs587784070
NM_022455.4(NSD1):c.1428G>A (p.Leu476=) rs587784072
NM_022455.4(NSD1):c.142A>G (p.Met48Val) rs200735877
NM_022455.4(NSD1):c.1471G>A (p.Glu491Lys) rs587784074
NM_022455.4(NSD1):c.1558G>A (p.Ala520Thr) rs559617787
NM_022455.4(NSD1):c.1805G>A (p.Cys602Tyr) rs797045806
NM_022455.4(NSD1):c.2399T>C (p.Met800Thr) rs142023792
NM_022455.4(NSD1):c.2450C>T (p.Ser817Phe) rs115722008
NM_022455.4(NSD1):c.2465C>G (p.Ser822Cys) rs377684553
NM_022455.4(NSD1):c.2835T>C (p.Ser945=) rs145987330
NM_022455.4(NSD1):c.2925C>T (p.Ser975=) rs587784090
NM_022455.4(NSD1):c.3000C>T (p.Ser1000=) rs150854966
NM_022455.4(NSD1):c.3267T>A (p.Asp1089Glu) rs1406037834
NM_022455.4(NSD1):c.3393C>T (p.Asn1131=) rs150296373
NM_022455.4(NSD1):c.3992A>G (p.Asp1331Gly) rs587784108
NM_022455.4(NSD1):c.4328A>G (p.Asn1443Ser) rs141911573
NM_022455.4(NSD1):c.4363A>G (p.Lys1455Glu) rs587784113
NM_022455.4(NSD1):c.4378+7A>G rs587784116
NM_022455.4(NSD1):c.4473G>T (p.Ser1491=) rs150920473
NM_022455.4(NSD1):c.4564G>T (p.Asp1522Tyr) rs201483724
NM_022455.4(NSD1):c.4966+15T>C rs587784130
NM_022455.4(NSD1):c.5520A>G (p.Glu1840=) rs140815139
NM_022455.4(NSD1):c.5809T>C (p.Ser1937Pro) rs587784159
NM_022455.4(NSD1):c.6001C>T (p.Leu2001=) rs587784172
NM_022455.4(NSD1):c.6152-14G>A rs587784182
NM_022455.4(NSD1):c.6259-8A>T rs370529039
NM_022455.4(NSD1):c.6637C>G (p.Leu2213Val) rs587784212
NM_022455.4(NSD1):c.6640G>A (p.Glu2214Lys) rs587784213
NM_022455.4(NSD1):c.6753A>G (p.Ser2251=) rs587784215
NM_022455.4(NSD1):c.7576C>T (p.Pro2526Ser) rs373932824
NM_022455.4(NSD1):c.7923T>C (p.Ala2641=) rs147033795

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