List of variants in gene CDC42 studied for hematologic disorder

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001791.4(CDC42):c.510C>T (p.Asp170=)	rs200782611	0.00001
NM_001791.4(CDC42):c.529C>T (p.Leu177=)	rs759623419	0.00001
NM_001791.4(CDC42):c.101C>A (p.Pro34Gln)	rs1645575465
NM_001791.4(CDC42):c.137T>C (p.Ile46Thr)	rs1570024112
NM_001791.4(CDC42):c.191A>G (p.Tyr64Cys)	rs864309721
NM_001791.4(CDC42):c.196A>G (p.Arg66Gly)	rs797044870
NM_001791.4(CDC42):c.203G>A (p.Arg68Gln)	rs1553196096
NM_001791.4(CDC42):c.206C>T (p.Pro69Leu)
NM_001791.4(CDC42):c.227A>T (p.Asp76Val)
NM_001791.4(CDC42):c.242G>T (p.Cys81Phe)	rs1553196100
NM_001791.4(CDC42):c.247T>C (p.Ser83Pro)	rs1553196101
NM_001791.4(CDC42):c.291G>T (p.Trp97Cys)
NM_001791.4(CDC42):c.511G>A (p.Glu171Lys)	rs1553196539
NM_001791.4(CDC42):c.62T>C (p.Ile21Thr)	rs1064795845
NM_001791.4(CDC42):c.68A>G (p.Tyr23Cys)	rs797044916

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.