ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_022455.4(NSD1):c.1482C>T (p.Cys494=) rs1363405
NM_022455.4(NSD1):c.1515T>C (p.Asn505=) rs114747882
NM_022455.4(NSD1):c.1749G>A (p.Glu583=) rs3733874
NM_022455.4(NSD1):c.1792T>C (p.Leu598=) rs28932176
NM_022455.4(NSD1):c.1811G>T (p.Arg604Leu) rs61744451
NM_022455.4(NSD1):c.1840G>T (p.Val614Leu) rs3733875
NM_022455.4(NSD1):c.2071G>A (p.Ala691Thr) rs28932177
NM_022455.4(NSD1):c.2176T>C (p.Ser726Pro) rs28932178
NM_022455.4(NSD1):c.2242A>G (p.Asn748Asp) rs587784083
NM_022455.4(NSD1):c.2295C>T (p.Asn765=) rs146767413
NM_022455.4(NSD1):c.3089T>C (p.Leu1030Ser) rs200856103
NM_022455.4(NSD1):c.3106G>C (p.Ala1036Pro) rs28932179
NM_022455.4(NSD1):c.3187A>G (p.Thr1063Ala) rs193290006
NM_022455.4(NSD1):c.3271C>A (p.Leu1091Ile) rs35597015
NM_022455.4(NSD1):c.352C>G (p.Pro118Ala) rs587784102
NM_022455.4(NSD1):c.3564G>C (p.Arg1188Ser) rs199814669
NM_022455.4(NSD1):c.3705T>C (p.Asn1235=) rs28932181
NM_022455.4(NSD1):c.3888A>G (p.Lys1296=) rs587784106
NM_022455.4(NSD1):c.395G>C (p.Cys132Ser) rs28932174
NM_022455.4(NSD1):c.4062C>T (p.Gly1354=) rs144562009
NM_022455.4(NSD1):c.4498-10del rs200890017
NM_022455.4(NSD1):c.4520C>T (p.Thr1507Met) rs144900277
NM_022455.4(NSD1):c.4564G>A (p.Asp1522Asn) rs201483724
NM_022455.4(NSD1):c.4883T>C (p.Met1628Thr) rs530920626
NM_022455.4(NSD1):c.5082C>T (p.Thr1694=) rs587784136
NM_022455.4(NSD1):c.5869C>T (p.Arg1957Trp) rs587784161
NM_022455.4(NSD1):c.6393C>G (p.Val2131=) rs587784194
NM_022455.4(NSD1):c.6444T>C (p.Asn2148=) rs146601031
NM_022455.4(NSD1):c.6750G>A (p.Met2250Ile) rs35848863
NM_022455.4(NSD1):c.6782T>C (p.Met2261Thr) rs34165241
NM_022455.4(NSD1):c.6903G>C (p.Gly2301=) rs11740250
NM_022455.4(NSD1):c.7391G>A (p.Arg2464His) rs587784216
NM_022455.4(NSD1):c.7403G>A (p.Arg2468Gln) rs587784217
NM_022455.4(NSD1):c.7597C>G (p.Leu2533Val) rs398124386
NM_022455.4(NSD1):c.7636G>A (p.Ala2546Thr) rs78247455
NM_022455.4(NSD1):c.7850T>C (p.Leu2617Ser) rs77618751
NM_022455.4(NSD1):c.7908C>T (p.Leu2636=) rs143159630

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