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

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2542695	NM_139239.5(NFKBID):c.1282C>A (p.His428Asn)	NFKBID (H301N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198008	NM_139239.5(NFKBID):c.1279G>A (p.Val427Ile)	NFKBID (V427I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525634	NM_139239.5(NFKBID):c.1205A>C (p.Gln402Pro)	NFKBID (Q260P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198002	NM_139239.5(NFKBID):c.1198C>G (p.Pro400Ala)	NFKBID (P258A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197999	NM_139239.5(NFKBID):c.1118G>A (p.Arg373Gln)	NFKBID (R383Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261833	NM_139239.5(NFKBID):c.1117C>T (p.Arg373Trp)	NFKBID (R246W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310946	NM_139239.5(NFKBID):c.764C>T (p.Ala255Val)	NFKBID (A265V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359988	NM_139239.5(NFKBID):c.761A>G (p.Asn254Ser)	NFKBID (N112S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345688	NM_139239.5(NFKBID):c.656G>A (p.Arg219His)	NFKBID (R77H +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2603979	NM_139239.5(NFKBID):c.653G>A (p.Arg218Gln)	NFKBID (R91Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197974	NM_139239.5(NFKBID):c.631G>T (p.Ala211Ser)	NFKBID (A211S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197969	NM_139239.5(NFKBID):c.601C>T (p.Arg201Trp)	NFKBID (R74W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361278	NM_139239.5(NFKBID):c.595G>A (p.Ala199Thr)	NFKBID (A57T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392611	NM_139239.5(NFKBID):c.592T>A (p.Phe198Ile)	NFKBID (F71I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance