"Ambry Genetics"[submitter] AND "MAP2K5"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3122785	NM_145160.3(MAP2K5):c.20G>T (p.Gly7Val)	MAP2K5 (G7V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122784	NM_145160.3(MAP2K5):c.198T>G (p.Asp66Glu)	MAP2K5 (D30E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122786	NM_145160.3(MAP2K5):c.295A>G (p.Ile99Val)	MAP2K5 (I63V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292975	NM_145160.3(MAP2K5):c.340G>A (p.Glu114Lys)	MAP2K5 (E78K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370341	NM_145160.3(MAP2K5):c.373C>T (p.Arg125Trp)	MAP2K5 (R89W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510964	NM_145160.3(MAP2K5):c.469G>A (p.Ala157Thr)	MAP2K5 (A121T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292977	NM_145160.3(MAP2K5):c.542A>G (p.Tyr181Cys)	MAP2K5 (Y181C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508055	NM_145160.3(MAP2K5):c.670A>G (p.Ile224Val)	MAP2K5 (I188V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122787	NM_145160.3(MAP2K5):c.698T>C (p.Val233Ala)	MAP2K5 (V233A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306794	NM_145160.3(MAP2K5):c.755A>G (p.Tyr252Cys)	MAP2K5 (Y252C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325653	NM_145160.3(MAP2K5):c.797C>T (p.Ala266Val)	MAP2K5 (A230V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535958	NM_145160.3(MAP2K5):c.1037T>C (p.Phe346Ser)	MAP2K5 (F310S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292978	NM_145160.3(MAP2K5):c.1090G>C (p.Gly364Arg)	MAP2K5 (G364R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122783	NM_145160.3(MAP2K5):c.1306C>T (p.Arg436Trp)	MAP2K5 (R400W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292976	NM_145160.3(MAP2K5):c.1307G>T (p.Arg436Leu)	MAP2K5 (R426L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292974	NM_145160.3(MAP2K5):c.1307G>A (p.Arg436Gln)	MAP2K5 (R436Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328258	NM_145160.3(MAP2K5):c.1331A>G (p.Gln444Arg)	MAP2K5 (Q434R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance