Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3321658221
- Species
- Rattus norvegicus
- Symbol
- rs3321658221
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Sox9
- Location
- 10:97806561
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- (mRatBN7.2)10:97806561T>G
- HGVS.c name
- ENSEMBL:ENSRNOT00000003511.7:c.-237T>G
- RefSeq:NM_080403.2:c.-237T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:97806485...97811994 (5.51 kb)
- Assembly version
- Not Available
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