List of variants in gene MPI reported as uncertain significance by Eurofins NTD LLC (GA)

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002435.3(MPI):c.303C>T (p.Leu101=)	rs139228075	0.00240
NM_002435.3(MPI):c.10C>T (p.Pro4Ser)	rs143982014	0.00133
NM_002435.3(MPI):c.748G>A (p.Gly250Ser)	rs748090636	0.00010
NM_002435.3(MPI):c.576C>T (p.Ser192=)	rs794727716
NM_002435.3(MPI):c.612T>G (p.Ser204Arg)	rs886043207
NM_002435.3(MPI):c.677C>T (p.Ala226Val)	rs727504018
NM_002435.3(MPI):c.678C>A (p.Ala226=)	rs199972529

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.