List of variants in gene DNMT3A studied for bone cancer

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_022552.5(DNMT3A):c.1903C>T (p.Arg635Trp)	rs144689354	0.00006
NM_022552.5(DNMT3A):c.2311C>T (p.Arg771Ter)	rs779626155	0.00004
NM_022552.5(DNMT3A):c.120G>A (p.Glu40=)	rs202118149	0.00001
NM_022552.5(DNMT3A):c.1035_1045del (p.Met345fs)	rs1573338559
NM_022552.5(DNMT3A):c.1676G>A (p.Cys559Tyr)	rs1313738991
NM_022552.5(DNMT3A):c.2204A>G (p.Tyr735Cys)	rs147828672
NM_022552.5(DNMT3A):c.2525A>G (p.Gln842Arg)	rs771174392
NM_022552.5(DNMT3A):c.2644C>A (p.Arg882Ser)	rs377577594
NM_022552.5(DNMT3A):c.2644C>G (p.Arg882Gly)	rs377577594
NM_022552.5(DNMT3A):c.2644C>T (p.Arg882Cys)	rs377577594
NM_022552.5(DNMT3A):c.2645G>A (p.Arg882His)	rs147001633
NM_022552.5(DNMT3A):c.2645G>C (p.Arg882Pro)	rs147001633
NM_022552.5(DNMT3A):c.2645G>T (p.Arg882Leu)	rs147001633
NM_022552.5(DNMT3A):c.2666T>G (p.Leu889Arg)
NM_022552.5(DNMT3A):c.656A>G (p.Lys219Arg)	rs950156492
NM_022552.5(DNMT3A):c.920C>T (p.Pro307Leu)	rs759380437

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