Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105170591
- Species
- Rattus norvegicus
- Symbol
- rs105170591
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Hspb2
- Location
- 8:51092852
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)8:51092852C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000013960.3:c.537+622G>A
- ENSEMBL:ENSRNOT00000100711.1:c.-193+591G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:51081342...51094533 (13.19 kb)
- Assembly version
- Not Available
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