"Ambry Genetics"[submitter] AND "LOC126861663"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3295217	NM_014938.6(MLXIP):c.713A>T (p.Asp238Val)	LOC126861663, MLXIP (D238V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334305	NM_014938.6(MLXIP):c.718G>C (p.Asp240His)	LOC126861663, MLXIP (D240H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528738	NM_014938.6(MLXIP):c.859T>C (p.Ser287Pro)	LOC126861663, MLXIP (S287P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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ClinVar