List of variants in gene DEPDC5 reported as uncertain significance by Athena Diagnostics Inc

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001242896.3(DEPDC5):c.4391C>T (p.Thr1464Met)	rs556147064	0.00019
NM_001242896.3(DEPDC5):c.130C>G (p.Pro44Ala)	rs756878843	0.00007
NM_001242896.3(DEPDC5):c.3085A>G (p.Thr1029Ala)	rs537257402	0.00006
NM_001242896.3(DEPDC5):c.380A>G (p.Tyr127Cys)	rs370881336	0.00004
NM_001242896.3(DEPDC5):c.2704G>A (p.Val902Ile)	rs374944205	0.00003
NM_001242896.3(DEPDC5):c.3461C>T (p.Ser1154Phe)	rs578244490	0.00003
NM_001242896.3(DEPDC5):c.1265G>A (p.Arg422Gln)	rs886039277	0.00001
NM_001242896.3(DEPDC5):c.1291G>A (p.Ala431Thr)	rs777844378
NM_001242896.3(DEPDC5):c.2416C>T (p.Arg806Cys)	rs953743301
NM_001242896.3(DEPDC5):c.3799G>A (p.Asp1267Asn)	rs1340279120
NM_001242896.3(DEPDC5):c.4262A>C (p.Glu1421Ala)	rs1555933874

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.