Related gene-specific medical variations for Gene (Select 1877) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3086789	NM_004424.5(E4F1):c.156A>C (p.Glu52Asp)	E4F1, LOC130058222 (E52D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086786	NM_004424.5(E4F1):c.111G>C (p.Leu37Phe)	E4F1, LOC130058222 (L37F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242487	NM_004424.5(E4F1):c.28A>T (p.Thr10Ser)	E4F1, LOC130058221 (T10S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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