"Ambry Genetics"[submitter] AND "NRBP1"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2508806	NM_013392.4(NRBP1):c.125C>G (p.Ser42Cys)	NRBP1 (S42C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300996	NM_013392.4(NRBP1):c.415A>G (p.Ile139Val)	NRBP1 (I139V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3300998	NM_013392.4(NRBP1):c.841T>G (p.Ser281Ala)	NRBP1 (S249A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272428	NM_013392.4(NRBP1):c.896T>C (p.Leu299Ser)	NRBP1 (L298S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300997	NM_013392.4(NRBP1):c.934C>T (p.Pro312Ser)	NRBP1 (P280S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300994	NM_013392.4(NRBP1):c.1004T>A (p.Leu335His)	NRBP1 (L303H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540091	NM_013392.4(NRBP1):c.1108C>T (p.Pro370Ser)	NRBP1 (P369S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299498	NM_013392.4(NRBP1):c.1229C>T (p.Pro410Leu)	NRBP1 (P378L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257863	NM_013392.4(NRBP1):c.1232G>A (p.Arg411Gln)	NRBP1 (R418Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478998	NM_013392.4(NRBP1):c.1361T>C (p.Val454Ala)	NRBP1 (V453A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300995	NM_013392.4(NRBP1):c.1412A>G (p.Lys471Arg)	NRBP1 (K470R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202026	NM_013392.4(NRBP1):c.1548C>A (p.Asn516Lys)	NRBP1 (N516K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance