Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs106269289
- Species
- Rattus norvegicus
- Symbol
- rs106269289
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Acbd7
- Location
- 17:74904813
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (mRatBN7.2)17:74904813G>T
- HGVS.c name
- ENSEMBL:ENSRNOT00000064609.3:n.1210+35G>T
- RefSeq:NM_001126079.1:c.13-104C>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:74903177...74909977 (6.80 kb)
- Assembly version
- Not Available
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