"Ambry Genetics"[submitter] AND "RPA2"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2265829	NM_002946.5(RPA2):c.805G>A (p.Ala269Thr)	RPA2 (A173T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155905	NM_002946.5(RPA2):c.786C>A (p.Asp262Glu)	RPA2 (D266E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528299	NM_002946.5(RPA2):c.686A>G (p.Asp229Gly)	RPA2 (D233G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155904	NM_002946.5(RPA2):c.685G>A (p.Asp229Asn)	RPA2 (D229N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155903	NM_002946.5(RPA2):c.652G>T (p.Ala218Ser)	RPA2 (A122S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597018	NM_002946.5(RPA2):c.547A>G (p.Ile183Val)	RPA2 (I183V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368797	NM_002946.5(RPA2):c.491A>G (p.Asn164Ser)	RPA2 (N164S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328131	NM_002946.5(RPA2):c.425T>G (p.Val142Gly)	RPA2 (V150G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155902	NM_002946.5(RPA2):c.353C>T (p.Thr118Ile)	RPA2 (T122I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379432	NM_002946.5(RPA2):c.176T>G (p.Leu59Trp)	RPA2 (L63W +2 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2537769	NM_002946.5(RPA2):c.115T>C (p.Ser39Pro)	RPA2 (S39P +2 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2262412	NM_002946.5(RPA2):c.38C>T (p.Ser13Leu)	RPA2 (S13L +2 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3315115	NM_002946.5(RPA2):c.35C>T (p.Ser12Phe)	RPA2 (S20F +2 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance