"PreventionGenetics, part of Exact Sciences"[submitter] AND "MAG"[gene - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2106374	NM_002361.4(MAG):c.15G>A (p.Thr5=)	MAG	Single nucleotide variant (synonymous variant +1 more)	Hereditary spastic paraplegia 75 +1 more	GLikely benign
Select item 706192	NM_002361.4(MAG):c.216G>C (p.Val72=)	MAG	Single nucleotide variant (synonymous variant)	MAG-related disorder +1 more	GLikely benign
Select item 424686	NM_002361.4(MAG):c.452C>T (p.Ala151Val)	MAG (A151V +1 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 75 +3 more	GConflicting classifications of pathogenicity
Select item 707298	NM_002361.4(MAG):c.753C>G (p.Ala251=)	MAG	Single nucleotide variant (synonymous variant)	MAG-related disorder +1 more	GLikely benign
Select item 707299	NM_002361.4(MAG):c.771G>A (p.Val257=)	MAG	Single nucleotide variant (synonymous variant)	MAG-related disorder +1 more	GLikely benign
Select item 706616	NM_002361.4(MAG):c.855C>T (p.Ala285=)	MAG	Single nucleotide variant (synonymous variant)	MAG-related disorder +1 more	GBenign/Likely benign
Select item 707741	NM_002361.4(MAG):c.966C>T (p.Val322=)	MAG	Single nucleotide variant (synonymous variant)	MAG-related disorder +1 more	GBenign/Likely benign
Select item 705599	NM_002361.4(MAG):c.1609C>T (p.Arg537Cys)	MAG (R512C +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 703976	NM_002361.4(MAG):c.1657A>C (p.Asn553His)	MAG (N553H +1 more)	Single nucleotide variant (missense variant)	MAG-related disorder +1 more	GBenign/Likely benign
Select item 703792	NM_002361.4(MAG):c.1836G>A (p.Thr612=)	MAG	Single nucleotide variant (synonymous variant +1 more)	MAG-related disorder +2 more	GLikely benign