Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs105699029
- Species
- Rattus norvegicus
- Symbol
- rs105699029
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Mei1
- Location
- 7:113624253
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051342.1:g.113624253T>C
- HGVS.c name
- ENSEMBL:ENSRNOT00000009428.6:c.2254-793T>C
- RefSeq:NM_001130555.1:c.2254-793T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:113590142...113643513 (53.37 kb)
- Assembly version
- Not Available
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