"GeneDx"[submitter] AND "CDK20"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151951	GRCh38/hg38 9q22.1(chr9:87960841-88287835)x3	CDK20, LINC03026 +1 more	Copy number gain	See cases	GLikely benign
Select item 1180189	NM_001039803.3(CDK20):c.*153C>T	CDK20	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1235349	NM_001039803.3(CDK20):c.688-214G>A	CDK20	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268959	NM_001039803.3(CDK20):c.564-44C>T	CDK20	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238802	NM_001039803.3(CDK20):c.378+19C>T	CDK20	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242501	NM_001039803.3(CDK20):c.189+23G>C	CDK20	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294593	NM_001039803.3(CDK20):c.123G>A (p.Glu41=)	CDK20	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1231765	NM_001039803.3(CDK20):c.76-20G>T	CDK20 (C32F)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1239713	NM_001039803.3(CDK20):c.76-66T>C	CDK20	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275313	NC_000009.12:g.87974587G>C	CDK20	Single nucleotide variant	not provided	GBenign
Select item 253402	GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic