"Ambry Genetics"[submitter] AND "SKP2"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3318749	NM_005983.4(SKP2):c.32A>C (p.Asp11Ala)	SKP2 (D11A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2594828	NM_005983.4(SKP2):c.77C>T (p.Ser26Phe)	SKP2 (S26F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3318748	NM_005983.4(SKP2):c.271A>G (p.Asn91Asp)	SKP2 (N91D)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3318750	NM_005983.4(SKP2):c.273C>G (p.Asn91Lys)	SKP2 (N91K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2239951	NM_005983.4(SKP2):c.544C>T (p.Arg182Cys)	SKP2 (R182C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340555	NM_005983.4(SKP2):c.725G>T (p.Gly242Val)	SKP2 (G242V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323774	NM_005983.4(SKP2):c.971A>C (p.Lys324Thr)	SKP2 (K324T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162691	NM_005983.4(SKP2):c.1076T>C (p.Ile359Thr)	SKP2 (I145T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551330	NM_005983.4(SKP2):c.1132C>G (p.Leu378Val)	SKP2 (L164V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249970	NM_005983.4(SKP2):c.1266T>A (p.Ser422Arg)	SKP2 (S208R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536258	NM_005983.4(SKP2):c.1271T>A (p.Leu424Gln)	SKP2 (L210Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371879	NM_005983.4(SKP2):c.*1825G>A	SKP2 (G360R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2454262	NM_005983.4(SKP2):c.*1939G>T	SKP2 (V398L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance