ClinVar Miner

List of variants in gene PTPN11 reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
NM_002834.4(PTPN11):c.1124A>G (p.Tyr375Cys) rs41299183
NM_002834.4(PTPN11):c.119A>G (p.Asp40Gly) rs397516795
NM_002834.4(PTPN11):c.1225-7A>G rs727504397
NM_002834.4(PTPN11):c.1226G>C (p.Gly409Ala) rs201247699
NM_002834.4(PTPN11):c.1366G>A (p.Val456Met) rs397516796
NM_002834.4(PTPN11):c.1374C>A (p.His458Gln) rs727504393
NM_002834.4(PTPN11):c.1382C>G (p.Ala461Gly) rs397509344
NM_002834.4(PTPN11):c.1594G>A (p.Glu532Lys) rs587778634
NM_002834.4(PTPN11):c.1678C>T (p.Leu560Phe) rs397516797
NM_002834.4(PTPN11):c.1713-5T>A rs876657964
NM_002834.4(PTPN11):c.1724A>G (p.Asp575Gly) rs397516799
NM_002834.4(PTPN11):c.333-3T>C rs146749153
NM_002834.4(PTPN11):c.348T>A (p.His116Gln) rs1482410266
NM_002834.4(PTPN11):c.392A>G (p.Lys131Arg) rs397516805
NM_002834.4(PTPN11):c.556C>T (p.Arg186Trp) rs143433437
NM_002834.4(PTPN11):c.652A>G (p.Thr218Ala) rs768555552
NM_002834.4(PTPN11):c.661A>T (p.Ile221Leu) rs397516806
NM_002834.4(PTPN11):c.858T>A (p.Asp286Glu) rs397516811
NM_002834.4(PTPN11):c.931A>G (p.Met311Val) rs774939392

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.