"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "LOC1268056 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2638409	NM_020765.3(UBR4):c.15062C>T (p.Pro5021Leu)	LOC126805640, UBR4 (P5021L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2638410	NM_020765.3(UBR4):c.15009-174G>A	LOC126805640, UBR4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2638411	NM_020765.3(UBR4):c.15009-175C>T	LOC126805640, UBR4	Single nucleotide variant (intron variant)	not provided	GBenign

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