List of variants in gene NIPA1 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_144599.5(NIPA1):c.*2070A>C	rs746614226	0.00072
NM_144599.5(NIPA1):c.681C>T (p.Leu227=)	rs200282898	0.00015
NM_144599.5(NIPA1):c.753G>C (p.Ala251=)	rs199718530	0.00013
NM_144599.5(NIPA1):c.*3127G>A	rs547238314	0.00007
NM_144599.5(NIPA1):c.291C>G (p.Pro97=)	rs199818530	0.00006
NM_144599.5(NIPA1):c.537C>T (p.Ile179=)	rs547634456	0.00006
NM_144599.5(NIPA1):c.759G>A (p.Glu253=)	rs781769053	0.00003
NM_144599.5(NIPA1):c.1336_1340del
NM_144599.5(NIPA1):c.3118_3127del
NM_144599.5(NIPA1):c.540G>A (p.Ala180=)
NM_144599.5(NIPA1):c.774G>T (p.Ser258=)	rs371993191
NM_144599.5(NIPA1):c.897G>A (p.Thr299=)	rs368507906

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