"Ambry Genetics"[submitter] AND "E2F6"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2303627	NM_198256.4(E2F6):c.821A>C (p.Glu274Ala)	E2F6 (E199A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086754	NM_198256.4(E2F6):c.773G>A (p.Ser258Asn)	E2F6 (S258N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274295	NM_198256.4(E2F6):c.683A>G (p.Asn228Ser)	E2F6 (N76S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086753	NM_198256.4(E2F6):c.616G>A (p.Ala206Thr)	E2F6 (A206T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286481	NM_198256.4(E2F6):c.447C>G (p.Asp149Glu)	E2F6 (D149E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086752	NM_198256.4(E2F6):c.397A>G (p.Asn133Asp)	E2F6 (N101D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274294	NM_198256.4(E2F6):c.340G>A (p.Asp114Asn)	E2F6 (D82N +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2228140	NM_198256.4(E2F6):c.323A>G (p.Asn108Ser)	E2F6 (N108S +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3086751	NM_198256.4(E2F6):c.296G>A (p.Arg99Gln)	E2F6 (R24Q +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2379904	NM_198256.4(E2F6):c.281C>T (p.Thr94Met)	E2F6 (T19M +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3086755	NM_198256.4(E2F6):c.92A>C (p.Asn31Thr)	E2F6 (N31T)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2304013	NM_198256.4(E2F6):c.86C>T (p.Pro29Leu)	E2F6 (P29L)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2320129	NM_198256.4(E2F6):c.73C>T (p.Arg25Trp)	E2F6 (R25W)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance