Related gene-specific medical variations for Gene (Select 8061) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3279479	NM_005438.5(FOSL1):c.55G>A (p.Gly19Ser)	FOSL1, LOC130006086 (G19S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279478	NM_005438.5(FOSL1):c.31A>G (p.Ser11Gly)	FOSL1, LOC130006086 (S11G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595032	NM_005438.5(FOSL1):c.13T>G (p.Phe5Val)	FOSL1, LOC130006086 (F5V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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