List of variants in gene DRC1 reported by Fulgent Genetics, Fulgent Genetics

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_145038.5(DRC1):c.36G>C (p.Pro12=)	rs116549039	0.00942
NM_145038.5(DRC1):c.992C>T (p.Thr331Ile)	rs143181834	0.00771
NM_145038.5(DRC1):c.1067C>T (p.Ala356Val)	rs78892546	0.00566
NM_145038.5(DRC1):c.2166+16_2166+17insA	rs546596010	0.00252
NM_145038.5(DRC1):c.2223A>C (p.Ter741Cys)	rs151184011	0.00149
NM_145038.5(DRC1):c.352C>T (p.Gln118Ter)	rs142371860	0.00031
NM_145038.5(DRC1):c.1418C>T (p.Ala473Val)	rs199574440	0.00029
NM_145038.5(DRC1):c.421T>G (p.Trp141Gly)	rs139583194	0.00023
NM_145038.5(DRC1):c.1913A>C (p.Lys638Thr)	rs142671417	0.00014
NM_145038.5(DRC1):c.1124G>A (p.Arg375His)	rs141347582	0.00011
NM_145038.5(DRC1):c.1391G>A (p.Arg464His)	rs200271366	0.00004
NM_145038.5(DRC1):c.1599+1G>A	rs146412095	0.00004
NM_145038.5(DRC1):c.109dup (p.Gln37fs)	rs750136163
NM_145038.5(DRC1):c.2079_2086del (p.Arg694fs)	rs1558457993
NM_145038.5(DRC1):c.2190_2193dup (p.Thr732fs)	rs763631774

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.