List of variants in gene MLXIPL reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_032951.3(MLXIPL):c.444C>G (p.Pro148=)	rs72649027	0.00529
NM_032951.3(MLXIPL):c.2521C>T (p.Arg841Trp)	rs66489924	0.00522
NM_032951.3(MLXIPL):c.573+7G>A	rs200438567	0.00354
NM_032951.3(MLXIPL):c.483+8G>A	rs72649026	0.00285
NM_032951.3(MLXIPL):c.594A>G (p.Glu198=)	rs138119872	0.00278
NM_032951.3(MLXIPL):c.22C>T (p.Leu8=)	rs557125342	0.00028
NM_032951.3(MLXIPL):c.1971G>A (p.Ala657=)	rs370408161	0.00019
NM_032951.3(MLXIPL):c.1821C>T (p.Ser607=)
NM_032951.3(MLXIPL):c.213C>T (p.Ser71=)
NM_032951.3(MLXIPL):c.711G>C (p.Pro237=)
NM_032951.3(MLXIPL):c.932C>T (p.Pro311Leu)
NM_032951.3(MLXIPL):c.966C>T (p.Ser322=)

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