Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs107495899
- Species
- Rattus norvegicus
- Symbol
- rs107495899
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Rbbp9
- Location
- 3:131932303
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051338.1:g.131932303C>T
- HGVS.c name
- RefSeq:XM_039104444.1:c.-30-1616G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:131925095...131939042 (13.95 kb)
- Assembly version
- Not Available
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