Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs198361266
- Species
- Rattus norvegicus
- Symbol
- rs198361266
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Depdc7
- Location
- 3:91114882
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051338.1:g.91114882G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000016677.6:c.73+6110C>T
- ENSEMBL:ENSRNOT00000111299.1:c.34+5768C>T
- 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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