"Ambry Genetics"[submitter] AND "FUBP1"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2536832	NM_003902.5(FUBP1):c.1802C>T (p.Thr601Ile)	FUBP1 (T600I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457620	NM_003902.5(FUBP1):c.1670C>T (p.Ala557Val)	FUBP1 (A556V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608276	NM_003902.5(FUBP1):c.1624G>A (p.Ala542Thr)	FUBP1 (A541T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097418	NM_003902.5(FUBP1):c.1517C>T (p.Ala506Val)	FUBP1 (A526V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252579	NM_003902.5(FUBP1):c.1481C>G (p.Pro494Arg)	FUBP1 (P493R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
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 2322141	NM_003902.5(FUBP1):c.1349C>T (p.Pro450Leu)	FUBP1 (P449L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2229463	NM_003902.5(FUBP1):c.1327A>G (p.Ile443Val)	FUBP1 (I463V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097417	NM_003902.5(FUBP1):c.1285A>T (p.Ile429Phe)	FUBP1 (I449F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219605	NM_003902.5(FUBP1):c.1285A>G (p.Ile429Val)	FUBP1 (I429V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488581	NM_003902.5(FUBP1):c.1127T>C (p.Leu376Pro)	FUBP1 (L375P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097416	NM_003902.5(FUBP1):c.1115C>A (p.Pro372Gln)	FUBP1 (P371Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097421	NM_003902.5(FUBP1):c.641G>A (p.Arg214Gln)	FUBP1 (R235Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394363	NM_003902.5(FUBP1):c.548C>T (p.Pro183Leu)	FUBP1 (P204L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097420	NM_003902.5(FUBP1):c.498G>T (p.Gln166His)	FUBP1 (Q166H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097419	NM_003902.5(FUBP1):c.443G>A (p.Cys148Tyr)	FUBP1 (C148Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485085	NM_003902.5(FUBP1):c.155C>T (p.Ser52Leu)	FUBP1 (S52L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance