List of variants in gene CTC1 reported as likely pathogenic for hereditary epidermal appendage anomaly

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: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_025099.6(CTC1):c.2923A>G (p.Arg975Gly)	rs199473678	0.00007
NM_025099.6(CTC1):c.2960G>A (p.Arg987Gln)	rs769617113	0.00003
NM_025099.6(CTC1):c.2758+1G>T	rs200609323	0.00002
NM_025099.6(CTC1):c.1818+1G>A	rs773716148	0.00001
NM_025099.6(CTC1):c.2385+2T>C	rs1597378045	0.00001
NM_025099.6(CTC1):c.2386-1G>A	rs199861310	0.00001
NM_025099.6(CTC1):c.2518C>T (p.Arg840Trp)	rs373905859	0.00001
NM_025099.6(CTC1):c.1077+1G>A
NM_025099.6(CTC1):c.1120G>T (p.Glu374Ter)	rs1987674659
NM_025099.6(CTC1):c.1207-1G>C
NM_025099.6(CTC1):c.1617+1G>T	rs1201400384
NM_025099.6(CTC1):c.2385+1G>C	rs2151508864
NM_025099.6(CTC1):c.3157-2A>C
NM_025099.6(CTC1):c.3221+1G>A	rs766644829
NM_025099.6(CTC1):c.3221+2T>C
NM_025099.6(CTC1):c.3387+1G>A	rs1242486415
NM_025099.6(CTC1):c.3387+1G>C
NM_025099.6(CTC1):c.3583C>T (p.Arg1195Ter)	rs199473682
NM_025099.6(CTC1):c.436-1G>A

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.