List of variants in gene NSD1 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NC_000005.10:(?_177131798)_(177300213_)?)del
NM_022455.5(NSD1):c.1310C>G (p.Ser437Ter)	rs121908067
NM_022455.5(NSD1):c.3536del (p.Glu1179fs)	rs1562213381
NM_022455.5(NSD1):c.3958C>T (p.Arg1320Ter)	rs121908070
NM_022455.5(NSD1):c.4977dup (p.Arg1660fs)	rs1562269320
NM_022455.5(NSD1):c.5997_5998insT (p.Thr2000fs)	rs1562295135
NM_022455.5(NSD1):c.6151+1G>A	rs1562296511
NM_022455.5(NSD1):c.6429C>G (p.His2143Gln)	rs121908068
NM_022455.5(NSD1):c.6450dup (p.Lys2151fs)	rs864309639
NM_022455.5(NSD1):c.6548G>C (p.Cys2183Ser)	rs121908069
NM_022455.5(NSD1):c.6605G>A (p.Cys2202Tyr)	rs121908071
NM_022455.5(NSD1):c.7968_7971del (p.Gln2656fs)	rs1562312238
NM_022455.5(NSD1):c.896del (p.Ser299fs)	rs1562099585

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