"Ambry Genetics"[submitter] AND "LOC126862932"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2368418	NM_153443.5(KIR3DL3):c.1061T>C (p.Val354Ala)	KIR3DL3, LOC126862932 (V354A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2263906	NM_153443.5(KIR3DL3):c.1084G>A (p.Gly362Arg)	KIR3DL3, LOC126862932 (G362R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306747	NM_153443.5(KIR3DL3):c.1127C>A (p.Pro376His)	KIR3DL3, LOC126862932 (P376H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115105	NM_153443.5(KIR3DL3):c.1155T>G (p.Asn385Lys)	KIR3DL3, LOC126862932 (N385K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356188	NM_153443.5(KIR3DL3):c.1162G>A (p.Val388Ile)	KIR3DL3, LOC126862932 (V388I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308101	NM_153443.5(KIR3DL3):c.1195C>G (p.Gln399Glu)	KIR3DL3, LOC126862932 (Q399E)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2269916	NM_153443.5(KIR3DL3):c.1210C>A (p.Pro404Thr)	KIR3DL3, LOC126862932 (P404T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404499	NM_153443.5(KIR3DL3):c.1216A>G (p.Thr406Ala)	KIR3DL3, LOC126862932 (T406A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance