Whole genome collections of SNP and short indel variants are available for 52 inbred strains. The variants are derived from Illumina short read sequencing data generated between 2013-2021 from a mixture of read lengths (100-150bp).
VCF Files
Reference Genome | Variants | Accession |
GRCm39 | SNPs | PRJEB53906 |
Indels | TBD | |
GRCm38 | SNPs/Indels | PRJEB43298 |
Interactive Queries
Some of our project partners have developed interactive portals for querying the variant catalogs:
- Mouse Genome Informatics – SNP browser
- Ensembl Genome Browser – see ‘Strain table’ under ‘Genetic variation’ on the left panel of the browser