"TET3-related disorder"[Disease/phenotype] AND "Rady Children's Instit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1301874	NM_001287491.2(TET3):c.789G>C (p.Ala263=)	TET3	Single nucleotide variant (synonymous variant)	TET3-related disorder	GUncertain significance
Select item 1343781	NM_001287491.2(TET3):c.3130-5C>T	TET3	Single nucleotide variant (intron variant)	TET3-related disorder	GUncertain significance
Select item 1343780	NM_001287491.2(TET3):c.3946G>C (p.Glu1316Gln)	TET3 (E1223Q +1 more)	Single nucleotide variant (missense variant)	TET3-related disorder	GUncertain significance

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