"MOG-related condition"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3056332	NM_206809.4(MOG):c.306A>G (p.Lys102=)	MOG	Single nucleotide variant (synonymous variant +1 more)	MOG-related condition	GLikely benign
Select item 3059372	NM_206809.4(MOG):c.511G>C (p.Val171Leu)	MOG (V171L +1 more)	Single nucleotide variant (missense variant)	MOG-related condition	GBenign
Select item 3060512	NM_206809.4(MOG):c.520A>G (p.Ile174Val)	MOG (I174V +1 more)	Single nucleotide variant (missense variant)	MOG-related condition	GBenign
Select item 3033947	NM_206809.4(MOG):c.730+65A>G	MOG	Single nucleotide variant (synonymous variant +1 more)	MOG-related condition	GLikely benign
Select item 3048015	NM_206809.4(MOG):c.730+147_730+149del	MOG (P293del)	Microsatellite (inframe deletion +1 more)	MOG-related condition	GBenign

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