"Ambry Genetics"[submitter] AND "ASF1A"[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2285206	NM_014034.3(ASF1A):c.47C>G (p.Ser16Cys)	ASF1A, MCM9 (S16C)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2489942	NM_014034.3(ASF1A):c.87G>T (p.Glu29Asp)	ASF1A, MCM9 (E29D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490756	NM_014034.3(ASF1A):c.366A>C (p.Leu122Phe)	ASF1A, MCM9 (L122F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3317927	NM_014034.3(ASF1A):c.430C>T (p.Pro144Ser)	ASF1A, MCM9 (P144S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313635	NM_014034.3(ASF1A):c.470C>T (p.Thr157Ile)	ASF1A, MCM9 (T157I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372468	NM_014034.3(ASF1A):c.485A>G (p.Asp162Gly)	ASF1A, MCM9 (D162G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223336	NM_014034.3(ASF1A):c.497G>A (p.Ser166Asn)	ASF1A, MCM9 (S166N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3317917	NM_014034.3(ASF1A):c.554G>A (p.Gly185Glu)	ASF1A, MCM9 (G185E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511204	NM_014034.3(ASF1A):c.583G>A (p.Val195Ile)	ASF1A, MCM9 (V195I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance