ClinVar Miner

List of variants reported as likely pathogenic for blood platelet disease by Hematology laboratory, Robert Debré Hospital

Included ClinVar conditions (105):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001130004.1(ACTN1):c.[2156A>C;2157G>C]
NM_001130004.2(ACTN1):c.1193A>C (p.Lys398Thr) rs1594768463
NM_001130004.2(ACTN1):c.1295C>T (p.Ala432Val) rs1594760140
NM_001130004.2(ACTN1):c.1348C>T (p.Arg450Cys) rs1594760036
NM_001130004.2(ACTN1):c.1349G>A (p.Arg450His) rs751173836
NM_001130004.2(ACTN1):c.1864C>T (p.His622Tyr) rs1594755688
NM_001130004.2(ACTN1):c.2243T>A (p.Met748Lys) rs1594751659
NM_001130004.2(ACTN1):c.770C>G (p.Thr257Arg) rs1594773549
NM_001130004.2(ACTN1):c.970A>G (p.Lys324Glu) rs1594771270
NM_001130004.2(ACTN1):c.982G>A (p.Val328Met) rs1594771236
NM_001130004.2(ACTN1):c.986A>G (p.Gln329Arg) rs1594771224

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.