"PreventionGenetics, part of Exact Sciences"[submitter] AND "CDC45"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 775656	NM_003504.5(CDC45):c.241G>A (p.Val81Ile)	CDC45 (V69I +1 more)	Single nucleotide variant (missense variant +2 more)	CDC45-related disorder +1 more	GBenign
Select item 777664	NM_003504.5(CDC45):c.365A>G (p.Asp122Gly)	CDC45 (D76G +2 more)	Single nucleotide variant (missense variant +1 more)	CDC45-related disorder +1 more	GLikely benign
Select item 1905670	NM_003504.5(CDC45):c.390T>C (p.Tyr130=)	CDC45	Single nucleotide variant (synonymous variant +1 more)	CDC45-related disorder +1 more	GLikely benign
Select item 1142614	NM_003504.5(CDC45):c.464A>G (p.Glu155Gly)	CDC45 (E109G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 716032	NM_003504.5(CDC45):c.542+130C>G	CDC45 (S183C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 735405	NM_003504.5(CDC45):c.705-5T>C	CDC45	Single nucleotide variant (intron variant)	CDC45-related disorder +1 more	GBenign/Likely benign
Select item 1344508	NM_003504.5(CDC45):c.1357G>A (p.Gly453Ser)	CDC45 (G407S +3 more)	Single nucleotide variant (missense variant)	CDC45-related disorder +1 more	GLikely benign
Select item 3050041	NM_003504.5(CDC45):c.1417C>T (p.Leu473=)	CDC45	Single nucleotide variant (synonymous variant)	CDC45-related disorder	GLikely benign

ClinVar