Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3318984395
- Species
- Rattus norvegicus
- Symbol
- rs3318984395
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2f8
- Location
- 1:98574056
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)1:98574056C>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000035512.7:c.947-115G>A
- RefSeq:NM_001100580.2:c.947-115G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:98565717...98584265 (18.55 kb)
- Assembly version
- Not Available
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