CDK7[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2296163	NM_001799.4(CDK7):c.7C>G (p.Leu3Val)	CDK7 (L3V)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GLikely benign
Select item 2463208	NM_001799.4(CDK7):c.80A>G (p.Tyr27Cys)	CDK7 (T16A +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2533920	NM_001799.4(CDK7):c.103A>T (p.Asn35Tyr)	CDK7 (N35Y)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2551928	NM_001799.4(CDK7):c.485T>C (p.Phe162Ser)	CDK7 (F162S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265504	NM_001799.4(CDK7):c.587T>C (p.Met196Thr)	CDK7 (M139T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329404	NM_001799.4(CDK7):c.799G>A (p.Asp267Asn)	CDK7 (D210N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar