"PreventionGenetics, part of Exact Sciences"[submitter] AND "DLL4"[gen - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1598777	NM_019074.4(DLL4):c.39A>T (p.Leu13=)	DLL4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 734190	NM_019074.4(DLL4):c.516G>C (p.Arg172=)	DLL4	Single nucleotide variant (synonymous variant)	DLL4-related disorder +1 more	GBenign/Likely benign
Select item 2630670	NM_019074.4(DLL4):c.572G>A (p.Arg191His)	DLL4 (R191H)	Single nucleotide variant (missense variant)	DLL4-related disorder	GLikely pathogenic
Select item 3030780	NM_019074.4(DLL4):c.658+3A>G	DLL4	Single nucleotide variant (intron variant)	DLL4-related disorder	GUncertain significance
Select item 713007	NM_019074.4(DLL4):c.672G>A (p.Ser224=)	DLL4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 725567	NM_019074.4(DLL4):c.897G>A (p.Thr299=)	DLL4	Single nucleotide variant (synonymous variant)	DLL4-related disorder +1 more	GBenign/Likely benign
Select item 2629923	NM_019074.4(DLL4):c.899G>A (p.Cys300Tyr)	DLL4 (C300Y)	Single nucleotide variant (missense variant)	DLL4-related disorder	GUncertain significance
Select item 1560240	NM_019074.4(DLL4):c.938G>A (p.Arg313His)	DLL4 (R313H)	Single nucleotide variant (missense variant)	DLL4-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 2217867	NM_019074.4(DLL4):c.1102G>A (p.Asp368Asn)	DLL4 (D368N)	Single nucleotide variant (missense variant)	DLL4-related disorder +1 more	GUncertain significance
Select item 3061616	NM_019074.4(DLL4):c.1254G>A (p.Leu418=)	DLL4	Single nucleotide variant (synonymous variant)	DLL4-related disorder	GLikely benign
Select item 2182187	NM_019074.4(DLL4):c.1320C>T (p.His440=)	DLL4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 737632	NM_019074.4(DLL4):c.1386C>T (p.Leu462=)	DLL4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign