"Ambry Genetics"[submitter] AND "ULBP1"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2369469	NM_025218.4(ULBP1):c.11C>T (p.Ala4Val)	ULBP1 (A4V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2241123	NM_025218.4(ULBP1):c.149G>A (p.Cys50Tyr)	ULBP1 (C50Y)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2277652	NM_025218.4(ULBP1):c.177G>C (p.Arg59Ser)	ULBP1 (R59S)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2296558	NM_025218.4(ULBP1):c.226T>A (p.Ser76Thr)	ULBP1 (S76T)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2367868	NM_025218.4(ULBP1):c.314T>A (p.Leu105Gln)	ULBP1 (L105Q)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2266078	NM_025218.4(ULBP1):c.370A>G (p.Arg124Gly)	ULBP1 (R124G)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2518079	NM_025218.4(ULBP1):c.403G>A (p.Gly135Ser)	ULBP1 (G135S)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2345904	NM_025218.4(ULBP1):c.454G>C (p.Asp152His)	ULBP1 (D152H)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2558336	NM_025218.4(ULBP1):c.461A>G (p.Asn154Ser)	ULBP1 (N154S)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2315395	NM_025218.4(ULBP1):c.536C>A (p.Thr179Asn)	ULBP1 (T179N)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2300346	NM_025218.4(ULBP1):c.543C>A (p.Phe181Leu)	ULBP1 (F181L)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2401891	NM_025218.4(ULBP1):c.694C>A (p.Leu232Ile)	ULBP1 (L52I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance