Variation Information: n4871

Name	n4871 View on WormBase
Species	C. elegans
Genetic position	IV:3.15 +/- 0.003 cM
Genomic position	genomic coordinates unknown or not listed
Protein change	protein change unknown or not listed

Strains carrying this variation

Strain	Genotype	Species	Description
MT15883	csp-2(n4871) IV.	C elegans	n4871 is a 1136 bp deletion that removes the last five exons, including the putative protease active site. Reference: Denning DP, et al. PLoS Genet. 2013;9(3):e1003341.