ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NM_022455.4(NSD1):c.140C>G (p.Thr47Ser) rs1562097679
NM_022455.4(NSD1):c.241A>G (p.Met81Val) rs763781326
NM_022455.4(NSD1):c.3224G>A (p.Gly1075Glu) rs1562212091
NM_022455.4(NSD1):c.5639G>A (p.Gly1880Asp) rs768219323
NM_022455.4(NSD1):c.682C>G (p.Pro228Ala)
NM_022455.4(NSD1):c.6848T>C (p.Leu2283Pro)
NM_022455.4(NSD1):c.7402C>T (p.Arg2468Trp)
NM_022455.4(NSD1):c.8014A>G (p.Lys2672Glu)
NM_022455.4(NSD1):c.887C>G (p.Pro296Arg) rs1189702665

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.