"Ambry Genetics"[submitter] AND "DNMT3L-AS1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2377742	NM_175867.3(DNMT3L):c.793C>T (p.Arg265Trp)	DNMT3L-AS1, DNMT3L (R265W)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2263229	NM_175867.3(DNMT3L):c.792C>A (p.His264Gln)	DNMT3L, DNMT3L-AS1 (H264Q)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance