Related gene-specific medical variations for Gene (Select 8880) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 777912	NM_003902.5(FUBP1):c.54T>C (p.Gly18=)	FUBP1, LOC129930801	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 134461	NM_003902.5(FUBP1):c.538G>T (p.Gly180Cys)	FUBP1 (G180C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134460	NM_003902.5(FUBP1):c.243A>C (p.Gln81His)	FUBP1 (Q81H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134459	NM_003902.5(FUBP1):c.1801A>G (p.Thr601Ala)	FUBP1 (T601A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134458	NM_003902.5(FUBP1):c.1588A>G (p.Thr530Ala)	FUBP1 (T530A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134457	NM_003902.5(FUBP1):c.1429C>T (p.Pro477Ser)	FUBP1 (P477S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 134456	NM_003902.5(FUBP1):c.992G>A (p.Arg331Gln)	FUBP1 (R331Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134455	NM_003902.5(FUBP1):c.56G>A (p.Gly19Asp)	FUBP1, LOC129930801 (G19D)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided

ClinVar