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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 293945	NM_001033044.4(GLUL):c.603+5G>A	GLUL, LOC126805944	Single nucleotide variant (intron variant)	GLUL-related condition +2 more	GLikely benign
Select item 293953	NM_001033044.4(GLUL):c.-14+997A>G	GLUL	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 293954	NM_001033044.4(GLUL):c.-14+958G>A	GLUL	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 293955	NM_001033044.4(GLUL):c.-14+955C>T	GLUL	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2639616	NM_001033044.4(GLUL):c.-14+913G>C	GLUL	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2639617	NM_001033044.4(GLUL):c.-14+850G>A	GLUL	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 624465	GRCh37/hg19 1q25.3(chr1:181863430-183148056)x1	DHX9, GLUL +9 more	Copy number loss	not provided	GUncertain significance

ClinVar