"PreventionGenetics, part of Exact Sciences"[submitter] AND "E2F1"[gen - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055516	NM_005225.3(E2F1):c.*5G>T	E2F1	Single nucleotide variant (3 prime UTR variant)	E2F1-related condition	GBenign
Select item 3050503	NM_005225.3(E2F1):c.1245C>T (p.Leu415=)	E2F1	Single nucleotide variant (synonymous variant)	E2F1-related condition	GLikely benign
Select item 3043057	NM_005225.3(E2F1):c.1239C>T (p.Phe413=)	E2F1	Single nucleotide variant (synonymous variant)	E2F1-related condition	GLikely benign
Select item 3041546	NM_005225.3(E2F1):c.1177G>A (p.Gly393Ser)	E2F1 (G393S)	Single nucleotide variant (missense variant)	E2F1-related condition	GBenign
Select item 3033085	NM_005225.3(E2F1):c.1176C>T (p.Ser392=)	E2F1	Single nucleotide variant (synonymous variant)	E2F1-related condition	GLikely benign
Select item 3043775	NM_005225.3(E2F1):c.1017C>T (p.Pro339=)	E2F1	Single nucleotide variant (synonymous variant)	E2F1-related condition	GLikely benign
Select item 719834	NM_005225.3(E2F1):c.826G>A (p.Val276Met)	E2F1 (V276M)	Single nucleotide variant (missense variant)	E2F1-related condition +1 more	GBenign
Select item 3037820	NM_005225.3(E2F1):c.741G>A (p.Thr247=)	E2F1	Single nucleotide variant (synonymous variant)	E2F1-related condition	GBenign
Select item 3041382	NM_005225.3(E2F1):c.598G>A (p.Gly200Ser)	E2F1 (G200S)	Single nucleotide variant (missense variant)	E2F1-related condition	GBenign
Select item 785835	NM_005225.3(E2F1):c.304G>A (p.Ala102Thr)	E2F1 (A102T)	Single nucleotide variant (missense variant)	E2F1-related condition +1 more	GLikely benign