Variation Information: n3098
| Name | n3098 View on WormBase |
|---|---|
| Species | C. elegans |
| Genetic position | X:21.59 +/- 0.000 cM |
| Genomic position | X: 14954042..14954042 |
| Protein change | Substitution |
Strains carrying this variation
| Strain | Genotype | Species | Description |
|---|---|---|---|
| MT8987 | pag-3(n3098) X. | C. elegans | Kinker Unc, neuronal lineage defects including lineage reiterations and abnormal corpse pattern in ventral cord. Allele causes W113 opal. |