ClinVar Miner

List of variants in gene PSTPIP1 reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP
NM_003978.5(PSTPIP1):c.1072G>C (p.Ala358Pro) rs749462900
NM_003978.5(PSTPIP1):c.1115C>T (p.Ala372Val) rs200188483
NM_003978.5(PSTPIP1):c.1151A>G (p.Asp384Gly) rs200771233
NM_003978.5(PSTPIP1):c.1207G>C (p.Gly403Arg) rs369113632
NM_003978.5(PSTPIP1):c.1208G>A (p.Gly403Glu) rs201572812
NM_003978.5(PSTPIP1):c.418-6C>A rs200018722
NM_003978.5(PSTPIP1):c.493G>A (p.Gly165Ser) rs762291063
NM_003978.5(PSTPIP1):c.799A>G (p.Ser267Gly) rs145239831
NM_003978.5(PSTPIP1):c.847C>T (p.Pro283Ser) rs774891463
NM_003978.5(PSTPIP1):c.856A>G (p.Asn286Asp) rs377437961

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.