"LINGO1-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3057649	NM_032808.7(LINGO1):c.1827C>T (p.Ala609=)	LINGO1	Single nucleotide variant (synonymous variant)	LINGO1-related disorder	GLikely benign
Select item 3033788	NM_032808.7(LINGO1):c.1668C>T (p.Thr556=)	LINGO1	Single nucleotide variant (synonymous variant)	LINGO1-related disorder	GLikely benign
Select item 778558	NM_032808.7(LINGO1):c.1575C>T (p.Pro525=)	LINGO1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 776935	NM_032808.7(LINGO1):c.1557C>T (p.Pro519=)	LINGO1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2645596	NM_032808.7(LINGO1):c.1359G>A (p.Pro453=)	LINGO1	Single nucleotide variant (synonymous variant)	LINGO1-related disorder +1 more	GLikely benign
Select item 2645597	NM_032808.7(LINGO1):c.1194G>A (p.Thr398=)	LINGO1	Single nucleotide variant (synonymous variant)	LINGO1-related disorder +1 more	GLikely benign
Select item 3057691	NM_032808.7(LINGO1):c.1008C>T (p.Tyr336=)	LINGO1	Single nucleotide variant (synonymous variant)	LINGO1-related disorder	GLikely benign
Select item 3052164	NM_032808.7(LINGO1):c.945G>A (p.Glu315=)	LINGO1	Single nucleotide variant (synonymous variant)	LINGO1-related disorder	GLikely benign
Select item 3038997	NM_032808.7(LINGO1):c.939G>T (p.Leu313=)	LINGO1	Single nucleotide variant (synonymous variant)	LINGO1-related disorder	GLikely benign
Select item 3057095	NM_032808.7(LINGO1):c.798G>A (p.Thr266=)	LINGO1	Single nucleotide variant (synonymous variant)	LINGO1-related disorder	GLikely benign
Select item 3051993	NM_032808.7(LINGO1):c.274G>A (p.Ala92Thr)	LINGO1 (A86T +1 more)	Single nucleotide variant (missense variant)	LINGO1-related disorder	GLikely benign
Select item 3043983	NM_032808.7(LINGO1):c.147C>T (p.Ser49=)	LINGO1	Single nucleotide variant (synonymous variant)	LINGO1-related disorder	GLikely benign
Select item 3056021	NM_032808.7(LINGO1):c.7-9C>T	LINGO1	Single nucleotide variant (intron variant)	LINGO1-related disorder	GBenign
Select item 3035775	NM_032808.7(LINGO1):c.6+9G>A	LINGO1	Single nucleotide variant (intron variant)	LINGO1-related disorder	GLikely benign
Select item 3049469	NM_032808.7(LINGO1):c.-4C>A	LINGO1	Single nucleotide variant (5 prime UTR variant +1 more)	LINGO1-related disorder	GLikely benign