List of variants in gene NSD1 reported as uncertain significance by Baylor Genetics

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_022455.5(NSD1):c.3404C>T (p.Pro1135Leu)	rs1021852466	0.00001
NM_022455.5(NSD1):c.1382C>T (p.Thr461Ile)	rs776330654
NM_022455.5(NSD1):c.2051T>G (p.Ile684Arg)	rs1281302772
NM_022455.5(NSD1):c.3418G>A (p.Val1140Ile)	rs1763367854
NM_022455.5(NSD1):c.3965G>C (p.Arg1322Pro)	rs750684515
NM_022455.5(NSD1):c.56C>T (p.Pro19Leu)	rs1756207246
NM_022455.5(NSD1):c.6632A>G (p.Asn2211Ser)	rs2127279586
NM_022455.5(NSD1):c.7159C>G (p.Pro2387Ala)	rs1416255762
NM_022455.5(NSD1):c.7648G>A (p.Glu2550Lys)	rs1180593710
NM_022455.5(NSD1):c.7922C>T (p.Ala2641Val)	rs1371700950

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.