ClinVar for Gene (Select 107984757) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2245952	NM_001025248.2(DUT):c.158T>C (p.Ile53Thr)	DUT, DUT-AS1 +1 more (I53T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 1336417	NM_001025248.2(DUT):c.280+9G>A	DUT, DUT-AS1 +1 more	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 146334	GRCh38/hg38 15q21.1-21.2(chr15:47460844-52494222)x1	AP4E1, ATP8B4 +190 more	Copy number loss	See cases	GPathogenic

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