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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 40

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HGVS	dbSNP	gnomAD frequency
NM_022455.5(NSD1):c.1482C>T (p.Cys494=)	rs1363405	0.36334
NM_022455.5(NSD1):c.6903G>C (p.Gly2301=)	rs11740250	0.16701
NM_022455.5(NSD1):c.2176T>C (p.Ser726Pro)	rs28932178	0.15259
NM_022455.5(NSD1):c.1749G>A (p.Glu583=)	rs3733874	0.12785
NM_022455.5(NSD1):c.1840G>T (p.Val614Leu)	rs3733875	0.12636
NM_022455.5(NSD1):c.3705T>C (p.Asn1235=)	rs28932181	0.10490
NM_022455.5(NSD1):c.6750G>A (p.Met2250Ile)	rs35848863	0.04785
NM_022455.5(NSD1):c.6782T>C (p.Met2261Thr)	rs34165241	0.04781
NM_022455.5(NSD1):c.3106G>C (p.Ala1036Pro)	rs28932179	0.02602
NM_022455.5(NSD1):c.7636G>A (p.Ala2546Thr)	rs78247455	0.02182
NM_022455.5(NSD1):c.2071G>A (p.Ala691Thr)	rs28932177	0.01809
NM_022455.5(NSD1):c.1515T>C (p.Asn505=)	rs114747882	0.00694
NM_022455.5(NSD1):c.1792T>C (p.Leu598=)	rs28932176	0.00477
NM_022455.5(NSD1):c.4520C>T (p.Thr1507Met)	rs144900277	0.00206
NM_022455.5(NSD1):c.2295C>T (p.Asn765=)	rs146767413	0.00196
NM_022455.5(NSD1):c.7850T>C (p.Leu2617Ser)	rs77618751	0.00188
NM_022455.5(NSD1):c.2835T>C (p.Ser945=)	rs145987330	0.00133
NM_022455.5(NSD1):c.3564G>C (p.Arg1188Ser)	rs199814669	0.00042
NM_022455.5(NSD1):c.3187A>G (p.Thr1063Ala)	rs193290006	0.00025
NM_022455.5(NSD1):c.7908C>T (p.Leu2636=)	rs143159630	0.00025
NM_022455.5(NSD1):c.4509G>A (p.Met1503Ile)	rs199574095	0.00020
NM_022455.5(NSD1):c.6444T>C (p.Asn2148=)	rs146601031	0.00019
NM_022455.5(NSD1):c.2339C>T (p.Ser780Leu)	rs201327209	0.00014
NM_022455.5(NSD1):c.3271C>A (p.Leu1091Ile)	rs35597015	0.00009
NM_022455.5(NSD1):c.7597C>G (p.Leu2533Val)	rs398124386	0.00008
NM_022455.5(NSD1):c.3089T>C (p.Leu1030Ser)	rs200856103	0.00007
NM_022455.5(NSD1):c.395G>C (p.Cys132Ser)	rs28932174	0.00006
NM_022455.5(NSD1):c.7403G>A (p.Arg2468Gln)	rs587784217	0.00004
NM_022455.5(NSD1):c.5082C>T (p.Thr1694=)	rs587784136	0.00002
NM_022455.5(NSD1):c.2242A>G (p.Asn748Asp)	rs587784083	0.00001
NM_022455.5(NSD1):c.352C>G (p.Pro118Ala)	rs587784102	0.00001
NM_022455.5(NSD1):c.4883T>C (p.Met1628Thr)	rs530920626	0.00001
NM_022455.5(NSD1):c.7391G>A (p.Arg2464His)	rs587784216	0.00001
NM_022455.5(NSD1):c.1811G>T (p.Arg604Leu)	rs61744451
NM_022455.5(NSD1):c.3888A>G (p.Lys1296=)	rs587784106
NM_022455.5(NSD1):c.4062C>T (p.Gly1354=)	rs144562009
NM_022455.5(NSD1):c.4498-10del	rs200890017
NM_022455.5(NSD1):c.4564G>A (p.Asp1522Asn)	rs201483724
NM_022455.5(NSD1):c.5869C>T (p.Arg1957Trp)	rs587784161
NM_022455.5(NSD1):c.6393C>G (p.Val2131=)	rs587784194

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