List of variants in gene DNMT3A reported as pathogenic by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022552.5(DNMT3A):c.1243C>T (p.Gln415Ter)	rs754223052	0.00001
NM_022552.5(DNMT3A):c.1367del (p.Lys456fs)
NM_022552.5(DNMT3A):c.2204A>G (p.Tyr735Cys)	rs147828672
NM_022552.5(DNMT3A):c.2644C>T (p.Arg882Cys)	rs377577594

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