Related gene-specific medical variations for Gene (Select 4135) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3293141	NM_033063.2(MAP6):c.2065G>A (p.Glu689Lys)	LOC105369391, MAP6 (E689K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123135	NM_033063.2(MAP6):c.2032G>C (p.Gly678Arg)	LOC105369391, MAP6 (G678R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557690	NM_033063.2(MAP6):c.2077G>A (p.Val693Ile)	LOC105369391, MAP6 (V693I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529132	NM_033063.2(MAP6):c.1940C>T (p.Pro647Leu)	LOC105369391, MAP6 (P647L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2517875	NM_033063.2(MAP6):c.1582G>A (p.Asp528Asn)	LOC105369391, MAP6 (D528N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355287	NM_033063.2(MAP6):c.1798T>C (p.Ser600Pro)	LOC105369391, MAP6 (S600P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2309798	NM_033063.2(MAP6):c.1408C>A (p.Leu470Ile)	LOC105369391, MAP6 (L470I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263956	NM_033063.2(MAP6):c.2002C>A (p.Pro668Thr)	LOC105369391, MAP6 (P668T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1289911	NM_033063.2(MAP6):c.1749T>C (p.Asp583=)	LOC105369391, MAP6	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 778541	NM_033063.2(MAP6):c.2340G>A (p.Lys780=)	LOC105369391, MAP6	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 252761	NM_033063.2(MAP6):c.2219G>A (p.Arg740His)	LOC105369391, MAP6 (R740H)	Single nucleotide variant (missense variant)	not specified	GLikely benign