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

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2596880	NM_138278.4(BNIPL):c.85A>G (p.Arg29Gly)	BNIPL (R29G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3134682	NM_138278.4(BNIPL):c.241C>T (p.Arg81Cys)	BNIPL (R81C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2392716	NM_138278.4(BNIPL):c.251G>A (p.Arg84His)	BNIPL (R2H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527102	NM_138278.4(BNIPL):c.277C>T (p.Arg93Trp)	BNIPL (R11W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391591	NM_138278.4(BNIPL):c.331G>A (p.Ala111Thr)	BNIPL (A111T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2602633	NM_138278.4(BNIPL):c.361C>A (p.Leu121Met)	BNIPL (L121M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367586	NM_138278.4(BNIPL):c.368T>C (p.Ile123Thr)	BNIPL (I123T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512097	NM_138278.4(BNIPL):c.491G>A (p.Arg164Gln)	BNIPL (R164Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2294220	NM_138278.4(BNIPL):c.524G>A (p.Gly175Glu)	BNIPL (G175E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488183	NM_138278.4(BNIPL):c.526C>T (p.His176Tyr)	BNIPL (H176Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322128	NM_138278.4(BNIPL):c.529C>T (p.His177Tyr)	BNIPL (H95Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134684	NM_138278.4(BNIPL):c.545G>A (p.Arg182Gln)	BNIPL (R100Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378600	NM_138278.4(BNIPL):c.565C>T (p.Arg189Cys)	BNIPL (R107C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379013	NM_138278.4(BNIPL):c.850C>T (p.Arg284Trp)	BNIPL (R284W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607147	NM_138278.4(BNIPL):c.1051C>T (p.Leu351Phe)	BNIPL (L269F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276307	NM_138278.4(BNIPL):c.1061C>T (p.Ser354Leu)	BNIPL (S354L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance