Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs3319974713
- Species
- Rattus norvegicus
- Symbol
- rs3319974713
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Depdc7
- Location
- 3:91100510
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)3:91100510C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000016677.6:c.1337-352G>A
- ENSEMBL:ENSRNOT00000111299.1:c.1298-352G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:91099111...91121152 (22.04 kb)
- Assembly version
- Not Available
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