ClinVar Miner

List of variants in gene NIPA1 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_144599.5(NIPA1):c.275C>T (p.Thr92Met)	rs765306724	0.00001
NM_144599.5(NIPA1):c.316G>A (p.Gly106Arg)	rs104894490
NM_144599.5(NIPA1):c.562A>G (p.Ile188Val)
NM_144599.5(NIPA1):c.773C>T (p.Ser258Leu)

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