"Ambry Genetics"[submitter] AND "LOC129931790"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2256260	NM_007240.3(DUSP12):c.25G>A (p.Asp9Asn)	DUSP12, LOC129931790 (D9N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086264	NM_007240.3(DUSP12):c.65G>C (p.Ser22Thr)	DUSP12, LOC129931790 (S22T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2481556	NM_007240.3(DUSP12):c.74G>A (p.Gly25Glu)	DUSP12, LOC129931790 (G25E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387487	NM_007240.3(DUSP12):c.184G>A (p.Glu62Lys)	DUSP12, LOC129931790 (E62K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329152	NM_007240.3(DUSP12):c.187G>A (p.Glu63Lys)	DUSP12, LOC129931790 (E63K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274043	NM_007240.3(DUSP12):c.191C>T (p.Pro64Leu)	DUSP12, LOC129931790 (P64L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366907	NM_007240.3(DUSP12):c.230G>A (p.Arg77His)	DUSP12, LOC129931790 (R77H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086261	NM_007240.3(DUSP12):c.259G>A (p.Glu87Lys)	DUSP12, LOC129931790 (E87K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar