List of variants in gene DNMT3A reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_022552.5(DNMT3A):c.89A>C (p.Glu30Ala)	rs143730975	0.00459
NM_022552.5(DNMT3A):c.801C>T (p.Ser267=)	rs116609083	0.00237
NM_022552.5(DNMT3A):c.1170C>T (p.Ser390=)	rs150182473	0.00138
NM_022552.5(DNMT3A):c.2151C>T (p.Asn717=)	rs141216815	0.00068
NM_022552.5(DNMT3A):c.-6G>A	rs148146288	0.00048
NM_022552.5(DNMT3A):c.1502A>G (p.Asn501Ser)	rs149738328	0.00035
NM_022552.5(DNMT3A):c.1155G>A (p.Pro385=)	rs368009374	0.00020
NM_022552.5(DNMT3A):c.2697C>T (p.Arg899=)	rs61758432	0.00013
NM_022552.5(DNMT3A):c.187G>A (p.Gly63Ser)	rs781108426	0.00001
NM_022552.5(DNMT3A):c.1929C>T (p.Ile643=)	rs906581890	0.00001
NM_022552.5(DNMT3A):c.1110C>T (p.Tyr370=)
NM_022552.5(DNMT3A):c.1152C>T (p.Phe384=)
NM_022552.5(DNMT3A):c.1488C>T (p.Ser496=)
NM_022552.5(DNMT3A):c.1611C>T (p.Cys537=)
NM_022552.5(DNMT3A):c.1827C>T (p.Phe609=)
NM_022552.5(DNMT3A):c.337G>A (p.Gly113Arg)

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