List of variants in gene WDR35 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 28

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020779.4(WDR35):c.2599G>A (p.Ala867Thr)	rs2293669	0.05563
NM_020779.4(WDR35):c.549C>T (p.Tyr183=)	rs34169020	0.03645
NM_020779.4(WDR35):c.1601G>A (p.Arg534Gln)	rs113345685	0.01206
NM_020779.4(WDR35):c.3019C>T (p.Arg1007Cys)	rs56395266	0.01130
NM_020779.4(WDR35):c.1089G>A (p.Thr363=)	rs79829477	0.00817
NM_020779.4(WDR35):c.2262C>T (p.Asp754=)	rs147206032	0.00285
NM_020779.4(WDR35):c.1470+131T>A	rs192330354	0.00277
NM_020779.4(WDR35):c.1591C>G (p.Leu531Val)	rs148242353	0.00233
NM_020779.4(WDR35):c.2066G>A (p.Arg689His)	rs74470618	0.00168
NM_020779.4(WDR35):c.1248T>G (p.Ile416Met)	rs144701688	0.00145
NM_020779.4(WDR35):c.1183A>T (p.Asn395Tyr)	rs143343508	0.00135
NM_020779.4(WDR35):c.1755C>T (p.Val585=)	rs146130105	0.00124
NM_020779.4(WDR35):c.1471-7A>G	rs376388391	0.00098
NM_020779.4(WDR35):c.3335A>G (p.Lys1112Arg)	rs138007924	0.00097
NM_020779.4(WDR35):c.770T>C (p.Val257Ala)	rs142955097	0.00095
NM_020779.4(WDR35):c.2149A>G (p.Ile717Val)	rs144493712	0.00089
NM_020779.4(WDR35):c.1227A>G (p.Thr409=)	rs148828104	0.00059
NM_020779.4(WDR35):c.3026C>G (p.Thr1009Arg)	rs201153804	0.00045
NM_020779.4(WDR35):c.2164C>T (p.Arg722Cys)	rs374073530	0.00011
NM_020779.4(WDR35):c.836A>G (p.Gln279Arg)	rs375814330	0.00004
NM_020779.4(WDR35):c.3170A>G (p.Tyr1057Cys)	rs541910371	0.00003
NM_020779.4(WDR35):c.932G>T (p.Trp311Leu)	rs200649783	0.00003
NM_020779.4(WDR35):c.1854T>G (p.Ile618Met)	rs767714993	0.00001
NM_020779.4(WDR35):c.2590G>A (p.Ala864Thr)	rs267607175	0.00001
NM_020779.4(WDR35):c.529A>G (p.Asn177Asp)	rs747028453	0.00001
NM_001006657.2(WDR35):c.1208T>C (p.Met403Thr)
NM_020779.4(WDR35):c.1058G>C (p.Arg353Pro)	rs76623454
NM_020779.4(WDR35):c.1401-14_1401-10del

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.