BCL2L14[gene] and "single gene"[properties] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2366535	NM_138723.2(BCL2L14):c.44A>G (p.Asp15Gly)	BCL2L14 (D15G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373462	NM_138723.2(BCL2L14):c.82G>A (p.Ala28Thr)	BCL2L14 (A28T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621704	NM_138723.2(BCL2L14):c.100C>T (p.His34Tyr)	BCL2L14 (H34Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275819	NM_138723.2(BCL2L14):c.124C>A (p.Leu42Ile)	BCL2L14 (L42I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494342	NM_138723.2(BCL2L14):c.167G>A (p.Arg56Lys)	BCL2L14 (R56K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 775306	NM_138723.2(BCL2L14):c.207G>A (p.Glu69=)	BCL2L14	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3133415	NM_138723.2(BCL2L14):c.214T>C (p.Trp72Arg)	BCL2L14 (W72R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3133416	NM_138723.2(BCL2L14):c.270G>T (p.Lys90Asn)	BCL2L14 (K90N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3133417	NM_138723.2(BCL2L14):c.332A>G (p.Lys111Arg)	BCL2L14 (K111R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399431	NM_138723.2(BCL2L14):c.503A>C (p.Gln168Pro)	BCL2L14 (Q168P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3133418	NM_138723.2(BCL2L14):c.513G>C (p.Gln171His)	BCL2L14 (Q171H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260654	NM_138723.2(BCL2L14):c.613G>A (p.Glu205Lys)	BCL2L14 (E205K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3133419	NM_138723.2(BCL2L14):c.638T>C (p.Val213Ala)	BCL2L14 (V213A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601897	NM_138723.2(BCL2L14):c.838G>A (p.Ala280Thr)	BCL2L14 (A280T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3260655	NM_138723.2(BCL2L14):c.850G>T (p.Ala284Ser)	BCL2L14 (A284S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620631	NM_138723.2(BCL2L14):c.854T>C (p.Ile285Thr)	BCL2L14 (I285T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533277	NM_138723.2(BCL2L14):c.873C>G (p.Asn291Lys)	BCL2L14 (N291K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339537	NM_138723.2(BCL2L14):c.956T>C (p.Leu319Pro)	BCL2L14 (L319P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211776	NM_138723.2(BCL2L14):c.976G>A (p.Val326Ile)	BCL2L14 (V326I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471968	NM_138723.2(BCL2L14):c.977T>C (p.Val326Ala)	BCL2L14 (V326A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 20