"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "NUB1"[gene - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2658190	NM_001243351.2(NUB1):c.240G>A (p.Thr80=)	NUB1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2658191	NM_001243351.2(NUB1):c.598+6C>T	NUB1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2583057	GRCh37/hg19 7q34-36.1(chr7:140154317-152551638)x1	C7orf33, CASP2 +125 more	Copy number loss	not provided	GPathogenic

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