List of variants in gene NSD1 reported as likely pathogenic by Neuberg Centre For Genomic Medicine, NCGM

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_022455.5(NSD1):c.1583del (p.Lys528fs)	rs2480445417
NM_022455.5(NSD1):c.2431_2432insCACTC (p.Ser811fs)	rs2480454936
NM_022455.5(NSD1):c.3940G>T (p.Glu1314Ter)	rs2480589884
NM_022455.5(NSD1):c.5268C>A (p.Tyr1756Ter)	rs2480720376
NM_022455.5(NSD1):c.5293G>T (p.Gly1765Ter)
NM_022455.5(NSD1):c.5972_5973dup (p.Asp1992fs)	rs2480788504
NM_022455.5(NSD1):c.6257dup (p.Asn2087fs)	rs2480811005

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